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  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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  • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
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  • C07D513/04—Ortho-condensed systems

Definitions

• the present application relates to novel compounds that selectively inhibit the activities of PI3K isoforms and their uses in therapeutic treatments.
• Phosphatidylinositol 3-kinase (PI 3-kinase or PI3K) is responsible for generating these phosphorylated signaling products.
• PI3K was initially identified as a protein associated with viral oncoproteins and growth factor receptor tyrosine kinases that phosphorylate phosphatidylinositol (PI) and its phosphorylated derivatives at the 3′-hydroxyl of the inositol ring (Panayotou et al., Trends Cell Biol., 2:358-60, 1992).
• Class I PI3Ks phosphorylate phosphatidylinositol (PI), phosphatidylinositol-4-phosphate, and phosphatidylinositol-4,5-biphosphate (PIP 2 ) to produce phosphatidylinositol-3-phosphate (PIP), phosphatidylinositol-3,4-biphosphate, and phosphatidylinositol-3,4,5-triphosphate, respectively.
• Class II PI3Ks phosphorylate PI and phosphatidylinositol-4-phosphate
• Class III PI3Ks phosphorylate PI.
• PI 3-kinase The initial purification and molecular cloning of PI 3-kinase revealed that it was a heterodimer consisting of p85 and p110 subunits (Otsu et al., Cell, 65:91-104, 1991; Hiles et al., Cell, 70:419-29, 1992). Later, four distinct Class I PI3Ks were identified and designated as PI3K ⁇ , ⁇ , ⁇ , and ⁇ isoforms. Each isoform consists of a distinct 110 kDa catalytic subunit and a regulatory subunit.
• the catalytic subunits of PI3K ⁇ , ⁇ , and ⁇ interacts, individually, with the same regulatory subunit p85, whereas the catalytic subunit of PI3K ⁇ (p110 ⁇ ) interacts with a distinct regulatory subunit p101.
• each PI3K isoform has distinct expression pattern.
• PIK3CA which encodes PI3K ⁇ is frequently mutated in human cancers (Engelman, Nat. Rev. Cancer, 9: 550-562, 2009).
• PI3K ⁇ is generally expressed in hematopoietic cells.
• PI3K isoforms are shown to be associated with proliferation or survival signaling in cancers, inflammatory, or autoimmune diseases. As each PI3K isoform has different biological function, PI3K isoforms are potential targets to treat cancer or disorder (U.S. Pat. Nos. 6,800,620; 8,435,988; 8,673,906; US Patent Application Publication No. US2013/0274253).
• the present application provides novel compounds that are inhibitors of PI3K isoforms.
• the application also provides compositions, including pharmaceutical compositions, kits that include the compounds, and methods of using and making the compounds.
• the compounds provided herein are useful in treating diseases, disorders, or conditions that are mediated by PI3K isoforms.
• the application also provides compounds for use in therapy.
• the application further provides compounds for use in a method of treating a disease, disorder, or condition that is mediated by PI3K isoforms.
• the application provides uses of the compounds in the manufacture of a medicament for the treatment of a disease, disorder or condition that is mediated by PI3K isoforms.
• X, Y and Z are independently selected from C(R′) or N, wherein at least one of X, Y, and Z is C(R′);
• n 0, 1, 2, 3, or 4;
• m′ is 0 or 1
• A is a single bond or C(O);
• each R′ is independently selected from hydrogen, halo, optionally substituted alkyl, optionally substituted haloalkyl, and optionally substituted cycloalkyl;
• each R 1 is independently selected from halo, cyano, optionally substituted C 1-6 alkyl, optionally substituted C 1-6 alkoxy, hydroxy, optionally substituted C 3-8 cycloalkyl, and optionally substituted sulfonyl;
• each R 2 is independently selected from halo, optionally substituted C 1-6 alkyl, optionally substituted C 1-6 haloalkyl, and optionally substituted C 3-8 cycloalkyl;
• R 3 is hydrogen, optionally substituted C 1-6 alkyl, optionally substituted C 3-8 cycloalkyl, or optionally substituted C 6-10 aryl;
• R 4 is a six- to twelve-membered heteroaryl having at least two heteroatoms, wherein each heteroatom is independently selected from N, O, or S, wherein the heteroaryl is optionally substituted with one, two, or three members independently selected from halo, cyano, —NH 2 , optionally substituted C 1-6 alkyl, optionally substituted C 2-6 alkynyl; and
• R 5 is hydrogen or optionally substituted C 1-6 alkyl; R 5 and R 3 together with the atoms to which they are attached optionally form a four- to eight-membered heterocyclic ring;
• A is a single bond or C(O);
• each R′ is independently selected from hydrogen, halo, C 1-4 alkyl, C 1-4 haloalkyl, or C 3-6 cycloalkyl, wherein the alkyl moiety is optionally substituted with C 1-4 alkoxy;
• each R 1 is independently selected from halo, cyano, C 1-4 alkyl, C 1-4 haloalkyl, or —SO 2 C 1-4 alkyl;
• each R 2 is independently selected from halo, C 1-4 alkyl, C 1-4 haloalkyl, or C 3-6 cycloalkyl, wherein the alkyl moiety is optionally substituted with C 1-4 alkoxy;
• R 3 is hydrogen, C 1-4 alkyl, C 3-6 cycloalkyl, or C 6-10 aryl; wherein the alkyl moiety is optionally substituted with hydroxyl or C 1-4 alkoxy, wherein C 1-4 alkoxy is optionally substituted with C 6-10 aryl;
• R 4 is a six- to twelve-membered heteroaryl having at least one aromatic ring and at least two nitrogen atoms, wherein the heteroaryl is optionally substituted with one, two, or three members independently selected from halo, cyano, —NH 2 , C 2-4 alkynyl, C 1-4 haloalkyl, and C 1-4 alkyl, wherein the C 2-4 alkynyl moiety is optionally substituted with C 6-10 aryl or C 3-8 heteroaryl, wherein each of the C 6-10 aryl and C 3-8 heteroaryl moieties is optionally substituted with one, two, or three members independently selected from halo and C 1-6 haloalkyl;
• R 5 is hydrogen or C 1-4 alkyl; R 5 and R 3 together with the nitrogen to which they are attached optionally form a five-membered heterocyclic ring;
• each R 1 is selected from fluoro, chloro, bromo, iodo, methyl, ethyl, propyl, butyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, cyano, methylsulfonyl, and ethylsulfonyl.
• each R 2 is selected from hydrogen, fluoro, chloro, bromo, iodo, methyl, ethyl, propyl, butyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, methoxymethyl, methoxyethyl, ethoxymethyl, methoxypropyl, ethoxyethyl, ethoxypropyl, cyclopropyl, and cyclobutyl.
• the compound of the present application having the structure of formula (I), wherein R 3 is selected from methyl, ethyl, propyl, cyclopropyl, cyclobutyl, phenyl, benzyloxymethyl, benzyloxyethyl, benzyloxypropyl, —CH 2 OH, —C 2 H 4 OH, or —C 3 H 6 OH.
• R 5 is selected from hydrogen, methyl, ethyl, or propyl.
• R 3 and R 5 together with the atoms to which they are attached optionally form pyrrolidinyl.
• R 4 is a monocyclic heteroaryl having at least two nitrogen atoms, wherein R 4 is optionally substituted with two to three members independently selected from the group consisting of halo, cyano, —NH 2 , C 1-4 alkyl, and optionally substituted C 2-4 alkynyl.
• R 4 is a bicyclic heteroaryl having at least one aromatic ring, at least two nitrogen atoms, and at least one additional heteroatom selected from N, O, or S, wherein R 4 is optionally substituted with one, two, or three members independently selected from the group consisting of halo, cyano, —NH 2 , and C 1-4 alkyl.
• R 4 is selected from purinyl, pyrimidinyl, pyrazinyl, pyridazinyl, thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, or imidazotriazinyl; wherein each moiety is optionally substituted with one, two, or three members selected from the group consisting of halo, cyano, —NH 2 , C 1-4 alkyl, C 2-4 alkynyl, wherein the C 2-4 alkynyl moiety is optionally substituted with C 6-10 aryl or C 4-8 heteroaryl, wherein each of the C 6-10 aryl or C 3-8 heteroaryl moieties is optionally substituted with one, two, or three members independently selected from fluoro, chloro, bromo, iodo, fluoromethyl, difluoromethyl, trifluoromethyl
• the PI3K inhibitors are the compounds selected from Table 1, a pharmaceutically acceptable salt, isomer, or a mixture thereof. In some embodiments, the PI3K inhibitors are the compounds selected from Table 1a, a pharmaceutically acceptable salt, isomer, or a mixture thereof. In additional embodiments, the compound is an (S)-enantiomer. In other embodiments, the compound is an (R)-enantiomer. In other additional embodiments, the compound is an atropisomer.
• the application also provides a pharmaceutical composition that comprises a compound of formula (I), a pharmaceutically acceptable salt, isomer, or a mixture thereof, together with at least one pharmaceutically acceptable vehicle.
• a pharmaceutically acceptable vehicle may be selected from carriers, adjuvants, and excipients.
• a method of treating a disease, disorder, or condition in a human in need thereof by administering to the human a therapeutically effective amount of a compound of formula (I) or a pharmaceutically acceptable salt, isomer, or a mixture thereof.
• a compound of formula (I) for use in a method of treating a disease, disorder or condition that is mediated by PI3K isoforms is also provided.
• the application also provides the use of a compound of formula (I) in the manufacture of a medicament for the treatment of a disease, disorder or condition that is mediated by PI3K isoforms.
• the disease, disorder, or condition is associated or mediated by PI3K.
• the disease, disorder, or condition is an inflammatory disorder.
• the disease, disorder, or condition is a cancer.
• Also provided herein is a method of inhibiting the activity of a phosphatidylinositol 3-kinase polypeptide by contacting the polypeptide with a compound of formula (I) or a pharmaceutically acceptable salt, isomer, or a mixture thereof.
• a method of inhibiting excessive or destructive immune reactions comprising administering an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt, isomer, or a mixture thereof.
• Also provided is a method of inhibiting growth or proliferation of cancer cells comprising contacting the cancer cells with an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt, isomer, or a mixture thereof.
• kits that includes a compound of formula (I) or a pharmaceutically acceptable salt, isomer, or a mixture thereof.
• the kit may further comprise a label and/or instructions for use of the compound in treating a disease, disorder, or condition in a human in need thereof.
• the disease, disorder, or condition may be associated or mediated by PI3K activity.
• articles of manufacture that include a compound of formula (I) or a pharmaceutically acceptable salt, isomer, or a mixture thereof, and a container.
• the container may be a vial, jar, ampoule, preloaded syringe, or an intravenous bag.
• a dash (“-”) that is not between two letters or symbols is used to indicate a point of attachment for a substituent. For example, —CONH 2 is attached through the carbon atom.
• a dash at the front or end of a chemical group is a matter of convenience; chemical groups may be depicted with or without one or more dashes without losing their ordinary meaning.
• a wavy line drawn through a line in a structure indicates a point of attachment of a group. Unless chemically or structurally required, no directionality is indicated or implied by the order in which a chemical group is written or named.
• C u-v indicates that the following group has from u to v carbon atoms.
• C 1-6 alkyl indicates that the alkyl group has from 1 to 6 carbon atoms.
• references to “about” a value or parameter herein includes (and describes) embodiments that are directed to that value or parameter per se.
• the term “about” includes the indicated amount ⁇ 10%.
• the term “about” includes the indicated amount ⁇ 5%.
• the term “about” includes the indicated amount ⁇ 1%.
• to the term “about X” includes description of “X”.
• the singular forms “a” and “the” include plural references unless the context clearly dictates otherwise.
• reference to “the compound” includes a plurality of such compounds and reference to “the assay” includes reference to one or more assays and equivalents thereof known to those skilled in the art.
• Alkyl refers to an unbranched or branched saturated hydrocarbon chain. As used herein, alkyl has 1 to 20 carbon atoms (i.e., C 1-20 alkyl), 1 to 8 carbon atoms (i.e., C 1-8 alkyl), 1 to 6 carbon atoms (i.e., C 1-6 alkyl), or 1 to 4 carbon atoms (i.e., C 1-4 alkyl).
• alkyl groups include methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, iso-butyl, tert-butyl, pentyl, 2-pentyl, isopentyl, neopentyl, hexyl, 2-hexyl, 3-hexyl, and 3-methylpentyl.
• butyl includes n-butyl, sec-butyl, isobutyl and t-butyl
• propyl includes n-propyl and isopropyl
• Alkenyl refers to an aliphatic group containing at least one carbon-carbon double bond and having from 2 to 20 carbon atoms (i.e., C 2-20 alkenyl), 2 to 8 carbon atoms (i.e., C 2-8 alkenyl), 2 to 6 carbon atoms (i.e., C 2-6 alkenyl), or 2 to 4 carbon atoms (i.e., C 2-4 alkenyl).
• alkenyl groups include ethenyl, propenyl, butadienyl (including 1,2-butadienyl and 1,3-butadienyl).
• Alkynyl refers to an aliphatic group containing at least one carbon-carbon triple bond and having from 2 to 20 carbon atoms (i.e., C 2-20 alkynyl), 2 to 8 carbon atoms (i.e., C 2-8 alkynyl), 2 to 6 carbon atoms (i.e., C 2-6 alkynyl), or 2 to 4 carbon atoms (i.e., C 2-4 alkynyl).
• alkynyl also includes those groups having one triple bond and one double bond.
• Alkoxy refers to the group “alkyl-O—”. Examples of alkoxy groups include methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, tert-butoxy, sec-butoxy, n-pentoxy, n-hexoxy, and 1,2-dimethylbutoxy.
• acyl refers to a group —C( ⁇ O)R, wherein R is hydrogen, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroalkyl, or heteroaryl; each of which may be optionally substituted, as defined herein.
• R is hydrogen, alkyl, cycloalkyl, heterocycloalkyl, aryl, heteroalkyl, or heteroaryl; each of which may be optionally substituted, as defined herein.
• Examples of acyl include formyl, acetyl, cyclohexylcarbonyl, cyclohexylmethyl-carbonyl, and benzoyl.
• “Amido” refers to both a “C-amido” group which refers to the group —C( ⁇ O)NR y R z and an “N-amido” group which refers to the group —NR y C( ⁇ O)R z , wherein R y and R z are independently selected from the group consisting of hydrogen, alkyl, aryl, haloalkyl, or heteroaryl; each of which may be optionally substituted.
• Amino refers to the group —NR y R z wherein R y and R z are independently selected from the group consisting of hydrogen, alkyl, haloalkyl, aryl, or heteroaryl; each of which may be optionally substituted.
• Aryl refers to an aromatic carbocyclic group having a single ring (e.g. monocyclic) or multiple rings (e.g. bicyclic or tricyclic) including fused systems.
• aryl has 6 to 20 ring carbon atoms (i.e., C 6-20 aryl), 6 to 12 carbon ring atoms (i.e., C 6-12 aryl), or 6 to 10 carbon ring atoms (i.e., C 6-10 aryl).
• Examples of aryl groups include phenyl, naphthyl, fluorenyl, and anthryl.
• Aryl does not encompass or overlap in any way with heteroaryl defined below. If one or more aryl groups are fused with a heteroaryl ring, the resulting ring system is heteroaryl.
• Cycloalkyl refers to a saturated or partially saturated cyclic alkyl group having a single ring or multiple rings including fused, bridged, and spiro ring systems.
• the term “cycloalkyl” includes cycloalkenyl groups (i.e. the cyclic group having at least one alkenyl).
• cycloalkyl has from 3 to 20 ring carbon atoms (i.e., C 3-20 cycloalkyl), 3 to 12 ring carbon atoms (i.e., C 3-12 cycloalkyl), 3 to 10 ring carbon atoms (i.e., C 3-10 cycloalkyl), 3 to 8 ring carbon atoms (i.e., C 3-8 cycloalkyl), or 3 to 6 ring carbon atoms (i.e., C 3-6 cycloalkyl).
• Examples of cycloalkyl groups include cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl.
• Halogen or “halo” includes fluoro, chloro, bromo, and iodo.
• Haloalkyl refers to an unbranched or branched alkyl group as defined above, wherein one or more hydrogen atoms are replaced by a halogen. For example, where a residue is substituted with more than one halogen, it may be referred to by using a prefix corresponding to the number of halogen moieties attached.
• Dihaloalkyl and trihaloalkyl refer to alkyl substituted with two (“di”) or three (“tri”) halo groups, which may be, but are not necessarily, the same halogen. Examples of haloalkyl include difluoromethyl (—CHF 2 ) and trifluoromethyl (—CF 3 ).
• Heteroalkyl refers to an alkyl group in which one or more of the carbon atoms (and any associated hydrogen atoms) are each independently replaced with the same or different heteroatomic group. By way of example, 1, 2 or 3 carbon atoms may be independently replaced with the same or different heteroatomic group. Heteroatomic groups include, but are not limited to, —NR—, —O—, —S—, —S(O)—, —S(O) 2 —, and the like, where R is H, alkyl, aryl, cycloalkyl, heteroalkyl, heteroaryl or heterocycloalkyl, each of which may be optionally substituted.
• heteroalkyl groups include —OCH 3 , —CH 2 OCH 3 , —SCH 3 , —CH 2 SCH 3 , —NRCH 3 , and —CH 2 NRCH 3 , where R is hydrogen, alkyl, aryl, arylalkyl, heteroalkyl, or heteroaryl, each of which may be optionally substituted.
• heteroalkyl include 1 to 10 carbon atoms, 1 to 8 carbon atoms, or 1 to 4 carbon atoms; and 1 to 3 heteroatoms, 1 to 2 heteroatoms, or 1 heteroatom.
• Heteroaryl refers to an aromatic group having a single ring, multiple rings, or multiple fused rings, with one or more ring heteroatoms independently selected from nitrogen, oxygen, and sulfur.
• heteroaryl include 1 to 20 ring carbon atoms (i.e., C 1-20 heteroaryl), 3 to 12 ring carbon atoms (i.e., C 3-12 heteroaryl), or 3 to 8 carbon ring atoms (i.e., C 3-8 heteroaryl); and 1 to 5 heteroatoms, 1 to 4 heteroatoms, 1 to 3 ring heteroatoms, 1 to 2 ring heteroatoms, or 1 ring heteroatom independently selected from nitrogen, oxygen, and sulfur.
• heteroaryl groups include pyrimidinyl, purinyl, pyridyl, pyridazinyl, benzothiazolyl, and pyrazolyl.
• Heteroaryl does not encompass or overlap with aryl as defined above.
• Heterocycloalkyl refers to a saturated or unsaturated cyclic alkyl group, with one or more ring heteroatoms independently selected from nitrogen, oxygen and sulfur.
• the term “heterocycloalkyl” includes heterocycloalkenyl groups (i.e. the heterocycloalkyl group having at least one alkenyl).
• a heterocycloalkyl may be a single ring or multiple rings wherein the multiple rings may be fused, bridged, or spiro.
• heterocycloalkyl has 2 to 20 ring carbon atoms (i.e., C 2-20 heterocycloalkyl), 2 to 12 ring carbon atoms (i.e., C 2-12 heterocycloalkyl), 2 to 10 ring carbon atoms (i.e., C 2-10 heterocycloalkyl), 2 to 8 ring carbon atoms (i.e., C 2-8 heterocycloalkyl), 3 to 12 ring carbon atoms (i.e., C 3-12 heterocycloalkyl), 3 to 8 ring carbon atoms (i.e., C 3-8 heterocycloalkyl), or 3 to 6 ring carbon atoms (i.e., C 3-6 heterocycloalkyl); having 1 to 5 ring heteroatoms, 1 to 4 ring heteroatoms, 1 to 3 ring heteroatoms, 1 to 2 ring heteroatoms, or 1 ring heteroatom independently selected from nitrogen, sulfur or oxygen.
• heterocycloalkyl groups include pyrrolidin
• “Hydroxy” or “hydroxyl” refers to the group —OH.
• Oxo refers to the group ( ⁇ O) or (O).
• “Sulfonyl” refers to the group —S(O) 2 R, where R is alkyl, haloalkyl, cycloalkyl, heterocycloalkyl, heteroaryl, or aryl. Examples of sulfonyl are methylsulfonyl, ethylsulfonyl, phenylsulfonyl, and toluenesulfonyl.
• a divalent group such as a divalent “alkyl” group, a divalent “aryl” group, etc.
• a divalent group such as a divalent “alkyl” group, a divalent “aryl” group, etc.
• combinations of groups are referred to herein as one moiety, e.g. arylalkyl, the last mentioned group contains the atom by which the moiety is attached to the rest of the molecule.
• substituted means that any one or more hydrogen atoms on the designated atom or group is replaced with one or more substituents other than hydrogen, provided that the designated atom's normal valence is not exceeded.
• the one or more substituents include, but are not limited to, alkyl, alkenyl, alkynyl, alkoxy, acyl, amino, amido, amidino, aryl, azido, carbamoyl, carboxyl, carboxyl ester, cyano, guanidino, halo, haloalkyl, heteroalkyl, heteroaryl, heterocycloalkyl, hydroxy, hydrazino, imino, oxo, nitro, alkylsulfinyl, sulfonic acid, alkylsulfonyl, thiocyanate, thiol, thione, or combinations thereof.
• substituents there may be one, two, three, four, five, or six substituents.
• Polymers or similar indefinite structures arrived at by defining substituents with further substituents appended ad infinitum e.g., a substituted aryl having a substituted alkyl which is itself substituted with a substituted aryl group, which is further substituted by a substituted heteroalkyl group, etc.
• substituents with further substituents appended ad infinitum e.g., a substituted aryl having a substituted alkyl which is itself substituted with a substituted aryl group, which is further substituted by a substituted heteroalkyl group, etc.
• the maximum number of serial substitutions in compounds described herein is three.
• serial substitutions of substituted aryl groups with two other substituted aryl groups are limited to substituted aryl (substituted aryl) substituted aryl.
• the above definitions are not intended to include impermissible substitution patterns (e.g., methyl substituted with 5 fluorines or heteroaryl groups having two adjacent oxygen ring atoms). Such impermissible substitution patterns are well known to the skilled artisan.
• substituted may describe other chemical groups defined herein.
• substituted aryl includes, but is not limited to, “alkylaryl.” Unless specified otherwise, where a group is described as optionally substituted, any substituents of the group are themselves unsubstituted.
• substituted alkyl refers to an alkyl group having one or more substituents including hydroxyl, halo, alkoxy, cycloalkyl, heterocycloalkyl, aryl, and heteroaryl.
• substituted cycloalkyl refers to a cycloalkyl group having one or more substituents including alkyl, haloalkyl, heterocycloalkyl, aryl, heteroaryl, alkoxy, halo, hydroxyl; “substituted aryl” refers to an aryl group having one or more substituents including halo, alkyl, haloalkyl, heterocycloalkyl, heteroaryl, alkoxy, and cyano, and “substituted sulfonyl” refers to a group —S(O) 2 R, in which R is substituted with one or more substituents of alkyl, cycloalkyl, heterocycloalkyl, aryl or heteroaryl.
• the one or more substituents may be further substituted with halo, alkyl, haloalkyl, alkoxy, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl, each of which is substituted.
• the substituents may be further substituted with halo, alkyl, haloalkyl, alkoxy, cycloalkyl, heterocycloalkyl, aryl, or heteroaryl, each of which is unsubstituted.
• the present application provides the compounds that function as inhibitors of PI3K isoforms.
• the PI3K inhibitors are the compounds having the structure of formula (J):
• W is CH or N
• X, Y and Z are independently selected from C(R′) or N, wherein at least one of X, Y, and Z is C(R′);
• n 0, 1, 2, 3, or 4;
• m′ is 0 or 1;
• A′ is OR 4 , N(R 5 )C(O)R 4 , or NR 5 R 4 ;
• each R′ is independently selected from hydrogen, halo, optionally substituted alkyl, optionally substituted haloalkyl, and optionally substituted cycloalkyl;
• each R 1 is independently selected from halo, cyano, optionally substituted alkyl, optionally substituted haloalkyl, optionally substituted alkoxy, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, and optionally substituted sulfonyl;
• each R 2 is independently selected from halo, optionally substituted alkyl, optionally substituted haloalkyl, and optionally substituted cycloalkyl;
• R 3 is hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, or optionally substituted aryl;
• R 4 is heteroaryl optionally substituted with one, two, or three members independently selected from halo, cyano, —NH 2 , optionally substituted alkyl, optionally substituted haloalkyl, and optionally substituted alkynyl; and
• R 5 is hydrogen or optionally substituted alkyl, wherein R 5 and R 3 together with the atoms to which they are attached optionally form a heterocyclic ring;
• the compounds have the formula (J), wherein
• W is CH or N
• X, Y and Z are independently selected from C(R′) or N, wherein at least one of X, Y, and Z is C(R′);
• n 0, 1, 2, 3, or 4;
• m′ is 0 or 1;
• A′ is OR 4 , N(R 5 )C(O)R 4 , or NR 5 R 4 ;
• each R′ is independently selected from hydrogen, halo, —NH 2 , optionally substituted alkyl, optionally substituted haloalkyl, and optionally substituted cycloalkyl;
• each R 1 is independently selected from halo, cyano, optionally substituted alkyl, optionally substituted haloalkyl, optionally substituted alkoxy, optionally substituted aryl, optionally substituted heteroaryl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, and optionally substituted sulfonyl;
• each R 2 is independently selected from halo, —NH 2 , optionally substituted alkyl, optionally substituted haloalkyl, and optionally substituted cycloalkyl;
• R 3 is hydrogen, optionally substituted alkyl, optionally substituted cycloalkyl, or optionally substituted aryl;
• R 4 is heteroaryl optionally substituted with one, two, or three members independently selected from halo, cyano, —NH 2 , optionally substituted alkyl, optionally substituted haloalkyl, and optionally substituted alkynyl; and
• R 5 is hydrogen or optionally substituted alkyl, wherein R 5 and R 3 together with the atoms to which they are attached optionally form a heterocyclic ring;
• the PI3K inhibitors are the compounds having the structure of formula (I):
• X, Y and Z are independently selected from C(R′) or N, wherein at least one of X, Y, and Z is C(R′);
• n 0, 1, 2, 3, or 4;
• m′ is 0 or 1
• A is a single bond or C(O);
• each R′ is independently selected from hydrogen, halo, optionally substituted alkyl, optionally substituted haloalkyl, and optionally substituted cycloalkyl;
• each R 1 is independently selected from halo, cyano, optionally substituted C 1-6 alkyl, optionally substituted C 1-6 alkoxy, hydroxy, optionally substituted C 3-8 cycloalkyl, and optionally substituted sulfonyl;
• each R 2 is independently selected from halo, optionally substituted C 1-6 alkyl, optionally substituted C 1-6 haloalkyl, and optionally substituted C 3-8 cycloalkyl;
• R 3 is hydrogen, optionally substituted C 1-6 alkyl, optionally substituted C 3-8 cycloalkyl, or optionally substituted C 6-10 aryl;
• R 4 is a six- to twelve-membered heteroaryl having at least two heteroatoms, wherein each heteroatom is independently selected from N, O, or S, wherein the heteroaryl is optionally substituted with one, two, or three members independently selected from halo, cyano, —NH 2 , optionally substituted C 1-6 alkyl, optionally substituted C 2-6 alkynyl; and
• R 5 is hydrogen or optionally substituted C 1-6 alkyl; R 5 and R 3 together with the atoms to which they are attached optionally form a four- to eight-membered heterocyclic ring;
• X, Y and Z are independently selected from C(R′) or N, wherein at least one of X, Y, and Z is N;
• n 1 or 2;
• m′ is 0 or 1
• A is a single bond or C(O);
• each R′ is independently selected from hydrogen, halo, C 1-4 alkyl, C 1-4 haloalkyl, or C 3-6 cycloalkyl, wherein the alkyl moiety is optionally substituted with C 1-4 alkoxy;
• each R 1 is independently selected from halo, cyano, C 1-4 alkyl, C 1-4 haloalkyl, and —SO 2 C 1-4 alkyl;
• each R 2 is independently selected from halo, C 1-4 alkyl, C 1-4 haloalkyl, and C 3-6 cycloalkyl, wherein the alkyl moiety is optionally substituted with C 1-4 alkoxy;
• R 3 is hydrogen, C 1-4 alkyl, C 3-6 cycloalkyl, or C 6-10 aryl; wherein the alkyl moiety is optionally substituted with hydroxyl or C 1-4 alkoxy, wherein C 1-4 alkoxy is optionally substituted with C 6-10 to aryl;
• R 4 is a six- to twelve-membered heteroaryl having at least one aromatic ring and at least two nitrogen atoms, wherein the heteroaryl is optionally substituted with 1 to 3 members independently selected from halo, cyano, —NH 2 , C 2-4 alkynyl, C 1-4 haloalkyl, and C 1-4 alkyl, wherein the C 2-4 alkynyl moiety is optionally substituted with C 6-10 aryl or C 3-8 heteroaryl, wherein each of the C 6-10 aryl and C 3-8 heteroaryl moieties is optionally substituted with halo or C 1-6 haloalkyl;
• R 5 is hydrogen or C 1-4 alkyl; R 5 and R 3 together with the nitrogen to which they are attached optionally form a five-membered heterocyclic ring;
• the compounds have the structure of formula (I), wherein
• X, Y and Z are independently selected from C(R′) or N, wherein at least one of X, Y, and Z is N;
• n 1 or 2;
• m′ is 0 or 1
• A is a single bond or C(O);
• each R′ is independently selected from hydrogen, halo, —NH 2 , C 1-4 alkyl, C 1-4 haloalkyl, or C 3-6 cycloalkyl, wherein the alkyl moiety is optionally substituted with C 1-4 alkoxy;
• each R 1 is independently selected from halo, cyano, C 1-4 alkyl, C 1-4 haloalkyl, and —SO 2 C 1-4 alkyl;
• each R 2 is independently selected from halo, —NH 2 , C 1-4 alkyl, C 1-4 haloalkyl, and C 3-6 cycloalkyl, wherein the alkyl moiety is optionally substituted with C 1-4 alkoxy;
• R 3 is hydrogen, C 1-4 alkyl, C 3-6 cycloalkyl, or C 6-10 aryl; wherein the alkyl moiety is optionally substituted with hydroxyl or C 1-4 alkoxy, wherein C 1-4 alkoxy is optionally substituted with C 6-10 aryl;
• R 4 is a six- to twelve-membered heteroaryl having at least one aromatic ring and at least two nitrogen atoms, wherein the heteroaryl is optionally substituted with 1 to 3 members independently selected from halo, cyano, —NH 2 , C 2-4 alkynyl, C 1-4 haloalkyl, and C 1-4 alkyl, wherein the C 2-4 alkynyl moiety is optionally substituted with C 6-10 aryl or C 3-8 heteroaryl, wherein each of the C 6-10 aryl and C 3-8 heteroaryl moieties is optionally substituted with halo or C 1-6 haloalkyl;
• R 5 is hydrogen or C 1-4 alkyl; R 5 and R 3 together with the nitrogen to which they are attached optionally form a five-membered heterocyclic ring;
• the compounds have the structure of formula (I), wherein
• each R 1 is selected from fluoro, chloro, bromo, iodo, methyl, ethyl, propyl, butyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, cyano, methylsulfonyl, and ethylsulfonyl;
• each R 2 is selected from hydrogen, fluoro, chloro, bromo, iodo, methyl, ethyl, propyl, butyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, methoxymethyl, methoxyethyl, ethoxymethyl, methoxypropyl, ethoxyethyl, ethoxypropyl, cyclopropyl, and cyclobutyl;
• R 3 is selected from methyl, ethyl, propyl, cyclopropyl, cyclobutyl, phenyl, benzyloxymethyl, benzyloxyethyl, benzyloxypropyl, —CH 2 OH, —C 2 H 4 OH, or —C 3 H 6 OH;
• R 5 is selected from hydrogen, methyl, ethyl, or propyl
• R 4 is selected from purinyl, pyrimidinyl, pyrazinyl, pyridazinyl, thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, or imidazotriazinyl; wherein each of the purinyl, pyrimidinyl, pyrazinyl, pyridazinyl, thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, or imidazotriazinyl moieties is optionally substituted with 1 to 3 members selected from the group consisting of halo, cyano, —NH 2 , C 1-4 alkyl, C 2-4 alkynyl, wherein the C 2-4 alkynyl moiety is optionally substituted with
• the compounds have the structure of formula (I), wherein
• each R 1 is selected from fluoro, chloro, bromo, iodo, methyl, ethyl, propyl, butyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, cyano, methylsulfonyl, and ethylsulfonyl;
• each R 2 is selected from hydrogen, fluoro, chloro, bromo, iodo, methyl, ethyl, propyl, butyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, methoxymethyl, methoxyethyl, ethoxymethyl, methoxypropyl, ethoxyethyl, ethoxypropyl, cyclopropyl, cyclobutyl, and —NH 2 ;
• R 3 is selected from methyl, ethyl, propyl, isopropyl, butyl, cyclopropyl, cyclobutyl, phenyl, benzyloxymethyl, benzyloxyethyl, benzyloxypropyl, —CH 2 OH, —C 2 H 4 OH, or —C 3 H 6 OH;
• R 5 is selected from hydrogen, methyl, ethyl, or propyl
• R 4 is selected from purinyl, pyrimidinyl, pyrazinyl, pyridazinyl, thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, imidazotriazinyl, or pyrazolopyrimidinyl; wherein each of the purinyl, pyrimidinyl, pyrazinyl, pyridazinyl, thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, imidazotriazinyl, or pyrazolopyrimidinyl moieties is optionally substituted with 1 to 3 members selected from the group consisting of halo, cyano, —NH 2 , C 1-4 alkyl, C 1-4 halo
• n, A, R 1 , R 2 , R 3 , R 4 , and R 5 are defined herein;
• n 0, 1, or 2;
• n, m, A, R 1 , R 2 , R 3 , R 4 , and R 5 are defined herein;
• n, m, A, R 1 , R 2 , R 3 , R 4 , and R 5 are defined herein;
• n, m, R 1 , R 2 , R 3 , and R 5 are defined herein;
• p 0, 1, 2, or 3;
• each R 4a is independently selected from halo, cyano, NH 2 , C 2-4 alkynyl, C 1-4 haloalkyl, and C 1-4 alkyl, wherein the C 2-4 alkynyl moiety is optionally substituted with C 6-10 aryl or C 3-8 heteroaryl, wherein each of the C 6-10 aryl and C 3-8 heteroaryl moieties is optionally substituted with one, two, or three members independently selected from halo and C 1-6 haloalkyl;
• n, m, p, R 1 , R 2 , R 3 , R 4a , and R 5 are defined herein;
• n, m, A, R 1 , R 2 , R 3 , R 4 , and R 5 are defined herein;
• n, m, p, R 1 , R 2 , R 3 , R 4a , and R 5 are defined herein;
• n, m, p, R 1 , R 2 , R 3 , R 4a , and R 5 are defined herein;
• n, m, A, R 1 , R 2 , R 3 , R 4 , and R 5 are defined herein;
• n, m, p, R 1 , R 2 , R 3 , R 4a , and R 5 are defined herein;
• n, m, p, R 1 , R 2 , R 3 , R 4a , and R 5 are defined herein;
• the compounds have the structure of any of formulae (IIa), (IIb), (IIIa), (IIIb), (IVa), or (IVb), wherein each R 4a is independently selected from halo, cyano, —NH 2 , C 2-4 alkynyl, C 1-4 haloalkyl, and C 1-4 alkyl, wherein the C 2-4 alkynyl moiety is optionally substituted with C 6-10 aryl or C 3-8 heteroaryl, wherein each of the C 6-10 aryl and C 3-8 heteroaryl moieties is optionally substituted with one, two, or three members independently selected from halo, and C 1-6 haloalkyl.
• each R 4a is independently selected from bromo, fluoro, chloro, cyano, —NH 2 , methyl, ethyl, propyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, and C 2-4 alkynyl, wherein the C 2-4 alkynyl moiety is optionally substituted with C 6-10 aryl or C 4-8 heteroaryl, wherein each of the C 6-10 aryl or C 3-8 heteroaryl moieties is optionally substituted with one or two members independently selected from fluoro, chloro, bromo, iodo, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, and trifluoroethyl.
• n is 0. In some embodiments, n is 1, 2, 3, or 4. In some embodiments, n is 1, 2, or 3. In other embodiments, n is 1 or 2. In certain embodiments, n is 1 and R 1 moiety may be located on any position of the phenyl of the quinazolinone ring. In another embodiment, n is 2. Both R 1 substituents or moieties may be the same or different. Two R 1 moieties may be located on any two positions of the phenyl of the quinazolinone ring. By way of example, the first R 1 may be ortho, meta, or para to the second R 1 . In yet another embodiment, n is 3.
• All R 1 substituents or moieties may be the same or different, or two R 1 may be the same and different from the third R 1 .
• Three R 1 moieties may be located on any three positions of the phenyl of the quinazolinone ring.
• the first R 1 may be ortho to the second R 1
• the first R 1 may be para to the third R 1 .
• n is 4.
• All R 1 substituents may be the same or different, three R 1 may be the same and different from the fourth R 1 , two R 1 may be the same and different from the third and the fourth R 1 .
• each R 1 is independently halo, cyano, optionally substituted C 1-6 alkyl, optionally substituted C 1-6 haloalkyl, optionally substituted C 1-6 alkoxy, hydroxy, optionally substituted C 3-6 cycloalkyl, optionally substituted C 3-6 heterocycloalkyl, optionally substituted C 6-10 aryl, optionally substituted C 4-8 heteroaryl, or optionally substituted C 1-6 alkylsulfonyl.
• each R 1 is independently halo, cyano, optionally substituted C 1-4 alkyl, optionally substituted C 1-4 haloalkyl, optionally substituted C 1-4 alkoxy, optionally substituted C 3-6 cycloalkyl, or optionally substituted C 1-4 alkylsulfonyl. In other embodiments, each R 1 is independently halo, cyano, C 1-4 haloalkyl, C 1-4 alkyl, or C 1-4 alkylsulfonyl.
• each R 1 is independently selected from fluoro, chloro, iodo, bromo, cyano, methyl, ethyl, propyl, butyl, fluoromethyl, fluoroethyl, difluoromethyl, difluoroethyl, trifluoromethyl, trifluoroethyl, methylsulfonyl, ethylsulfonyl, or propylsulfonyl.
• each R 1 is independently fluoro, chloro, iodo, cyano, methyl, ethyl, difluoromethyl (—CHF 2 ), trifluoromethyl (—CF 3 ), methoxy, methylsulfonyl (—SO 2 CH 3 ), cyclopropylmethyl, or cyclopropyl.
• each R 1 is independently fluoro, chloro, cyano, methylsulfonyl, methyl, or trifluoromethyl.
• m is 0. In some embodiments, m is 1, 2, or 3. In certain other embodiment, m is 1 or 2. In yet other embodiment, m is 1 and R 2 substituent or moiety may be located on any position of the ring. In the embodiment where m is 2, both R 2 substituents may be the same or different. Two R 2 moieties may be located on any two positions of the ring. For example, the first R 2 may be ortho to the second R 2 , and the first R 2 may be para to the third R 2 . In embodiments where m is 3, all three R 2 may be the same or different, or two R 2 may be the same and different from the third R 2 . Three R 2 moieties may be located on any three positions of the ring. It is understood that when two of X, Y, and Z are N, m may be 0, 1, or 2.
• m′ is 0. In some embodiments, m′ is 1 and R 2 may be located on the position of the carbon ring atom (e.g. not X, Y, or Z wherein one of X, Y, or Z is the attachment point to the quinazolinone ring) on the ring.
• each R 2 is independently selected from halo, optionally substituted alkyl, optionally substituted haloalkyl, and optionally substituted cycloalkyl. In some embodiments, each R 2 is independently halo, C 1-4 haloalkyl, C 3-6 cycloalkyl, or C 1-4 alkyl optionally substituted with C 1-4 alkoxy.
• each R 2 is independently fluoro, chloro, iodo, bromo, —CH 2 F, —CHF 2 , —CF 3 , fluoroethyl, difluoroethyl, trifluoroethyl, fluoropropyl, difluoropropyl, trifluoropropyl, methyl, ethyl, propyl, butyl, methoxymethyl, methoxyethyl, ethoxymethyl, methoxypropyl, ethoxyethyl, ethoxypropyl, cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl.
• each R 2 is independently fluoro, chloro, methyl, —CH 2 F, —CHF 2 , —CF 3 , methoxyethyl, or cyclopropyl.
• R 3 is hydrogen, optionally substituted C 1-6 alkyl, optionally substituted C 3-8 cycloalkyl, or optionally substituted C 6-10 aryl. In one embodiment, R 3 is hydrogen, C 3-6 cycloalkyl, C 6-10 aryl, or C 1-4 alkyl optionally substituted with hydroxy, C 6-10 arylC 1-4 alkoxy, or C 3-6 cycloalkyl.
• R 3 is hydrogen, methyl, ethyl, propyl, butyl, cyclopropylmethyl, cyclopropylethyl, cyclobutylmethyl, cyclobutylethyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, —CH 2 OH, —C 2 H 4 OH, —C 3 H 6 OH, benzyloxymethyl
• R 5 is hydrogen or optionally substituted C 1-6 alkyl. In some embodiments, R 5 is hydrogen or C 1-4 alkyl. In certain embodiments, R 5 is hydrogen, methyl, ethyl, propyl or butyl. In certain other embodiments, R 5 is hydrogen.
• R 3 and R 5 with the atoms to which they are attached optionally form a heterocyclic ring.
• the R 3 -R 5 heterocyclic ring is a three- to eight-membered heterocycloalkyl (i.e. heterocycloalkyl having three to eight ring members and at least one ring member is a heteroatom).
• the R 3 -R 5 heterocyclic ring is a four- to seven-membered heterocycloalkyl (i.e. heterocycloalkyl having four to seven ring members and at least one ring member is a heteroatom).
• the R 3 -R 5 heterocyclic ring is optionally substituted with halo.
• the R 3 -R 5 heterocyclic ring is a five-membered heterocycloalkyl.
• the R 3 -R 5 heterocyclic ring is C 3-8 heterocycloalkyl.
• the R 3 -R 5 heterocyclic ring is azepanyl, azetidinyl, piperidinyl, or pyrrolidinyl.
• the R 3 -R 5 heterocyclic ring is pyrrolidinyl.
• the R 3 -R 5 heterocyclic ring is a five-membered heterocycloalkyl substituted with halo. In other additional embodiments, the R 3 -R 5 heterocyclic ring is pyrrolidinyl substituted with fluoro, chloro, bromo, or iodo.
• R 4 is heteroaryl having at least two nitrogen atoms and at least one aromatic ring and R 4 heteroaryl is optionally substituted one, two, or three members independently selected from halo, cyano, —NH 2 , C 1-6 alkyl, and C 1-6 haloalkyl.
• R 4 heteroaryl is a six- to twelve-membered heteroaryl (i.e. heteroaryl having six to twelve ring members).
• R 4 heteroaryl may be a monocyclic or bicyclic heteroaryl.
• R 4 heteroaryl is a monocyclic heteroaryl having at least two nitrogen atoms.
• R 4 heteroaryl is a bicyclic heteroaryl having at least one aromatic ring, at least two nitrogen atoms, and at least one additional heteroatom selected from N, O, or S.
• R 4 heteroaryl is selected from purinyl, pyrimidinyl, thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, and imidazotriazinyl.
• R 4 heteroaryl is selected from purinyl, pyrimidinyl, thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, imidazotriazinyl, and pyrazolopyrimidinyl. In some other embodiment, R 4 heteroaryl is pyrazolopyrimidinyl.
• R 4 is heteroaryl optionally substituted with one, two, or three members independently selected from halo, cyano, —NH 2 , C 1-6 alkyl, C 1-6 haloalkyl, C 2-6 alkynyl, wherein C 2-6 alkynyl is optionally substituted with C 6-10 aryl or C 4-8 heteroaryl, wherein each of the C 6-10 aryl or C 3-8 heteroaryl moieties is optionally substituted with one, two, or three members independently selected from fluoro, chloro, bromo, iodo, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, and trifluoroethyl, wherein the R 4 heteroaryl is selected from the group consisting of
• R 4 heteroaryl is selected from the group consisting of
• R 4 heteroaryl is optionally substituted with C 2-6 alkynyl optionally substituted with C 6-10 aryl or C 4-8 heteroaryl, each of which is optionally substituted with halo or C 1-6 haloalkyl.
• R 4 is heteroaryl optionally substituted with one member of C 2-6 alkynyl substituted with C 6-10 aryl or C 4-8 heteroaryl, wherein each of the C 6-10 aryl or C 3-8 heteroaryl moieties is optionally substituted with one member selected from fluoro, chloro, bromo, iodo, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, and trifluoroethyl.
• R 4 heteroaryl is optionally substituted with one to three members independently selected from fluoro, chloro, bromo, iodo, cyano, methyl, ethyl, propyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, —NH 2 , and —C ⁇ C optionally substituted with
• R 4 is selected from purinyl, pyrimidinyl, thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, and imidazotriazinyl, each of which is optionally substituted with one, two, or three members independently selected from chloro, fluoro, bromo, iodo, methyl, ethyl, propyl, cyano, and —NH 2 .
• R 4 is selected from purinyl, pyrimidinyl, isothiazolopyrimidinyl, thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, imidazotriazinyl, and pyrazolopyrimidinyl, each of which is optionally substituted with one, two, or three members independently selected from chloro, fluoro, bromo, iodo, methyl, ethyl, propyl, cyano, —NH 2 , fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, and trifluoroethyl.
• R 4 is selected from thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, and imidazotriazinyl, each of which is optionally substituted with one or two members independently selected from chloro, fluoro, bromo, iodo, methyl, ethyl, propyl, and —NH 2 .
• R 4 is selected from thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, and imidazotriazinyl, each of which is optionally substituted with two members independently selected from chloro, fluoro, bromo, iodo, methyl, ethyl, propyl, and —NH 2 .
• R 4 is selected from thiazolopyrimidinyl, pyridopyrimidinyl, thienopyrimidinyl, pyrrolopyrimidinyl, furopyrimidinyl, and imidazotriazinyl, each of which is optionally substituted with one member selected from chloro, fluoro, bromo, iodo, and —NH 2 .
• R 4 is pyrimidinyl or pyrazinyl and R 4 is optionally substituted with at least one —NH 2 .
• R 4 is pyrimidinyl or pyrazinyl, each substituted with two or three members independently selected from chloro, fluoro, bromo, iodo, methyl, ethyl, propyl, cyano, and —NH 2 , and at least one of the two or three members is —NH 2 .
• R 4 is pyrimidinyl or pyrazinyl, each substituted with two or three members independently selected from chloro, fluoro, bromo, iodo, methyl, ethyl, propyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, cyano, and —NH 2 , and at least one of the two or three members is —NH 2 .
• R 4 is isothiazolopyrimidinyl or pyrazolopyrimidinyl, each substituted with two or three members independently selected from chloro, fluoro, bromo, iodo, methyl, ethyl, propyl, cyano, —NH 2 , fluoromethyl, difluoromethyl, and trifluoromethyl, fluoroethyl, difluoroethyl, trifluoroethyl, and at least one of the two or three members is —NH 2 .
• A is C(O). In certain embodiments, A is a single bond. Each and every variation of A may be combined with each and every variation of n, m′, m, X, Y, Z, R′, R 1 , R 2 , R 3 , R 4 , and R 5 as described above. In some other embodiments, A is C(O) and R 4 heteroaryl is a bicyclic group defined above. In other embodiments, A is a single bond and R 4 heteroaryl is a bicyclic group defined above. In additional embodiments, A is C(O) and R 4 heteroaryl is a monocyclic group selected from pyrimidinyl and pyrazinyl. In other embodiments, A is a single bond and R 4 heteroaryl is a monocyclic group selected from pyrimidinyl and pyrazinyl.
• A′ is OR 4 . In some further embodiments, A′ is N(R 5 )C(O)R 4 . In yet further embodiments, A′ is NR 5 R 4 . Each and every variation of A′ may be combined with each and every variation of n, m′, X, Y, Z, R′, R 1 , R 2 , R 3 , R 4 , and R 5 as described above.
• X, Y, and Z are independently C(R′) or N, wherein at least one of X, Y, and Z is C(R′).
• X, Y, and Z are independently C(R′) or N, wherein at least one of X, Y, and Z is C(R′).
• all of X, Y, and Z are C(R′). In some embodiments, at least two of X, Y, and Z are C(R′). In other embodiments, at least one of X, Y, or Z is C(R′). In certain other embodiments, at least two of X, Y, and Z are N. In some other embodiments, at least one of X, Y, and Z is N. It is understood that R′ may be an attachment point to the quinazolinone ring. In such embodiments, X, Y, or Z is the attachment point to the quinazolinone ring by the R′ attachment.
• R′ is independently halo, optionally substituted alkyl, optionally substituted haloalkyl, and optionally substituted cycloalkyl.
• each R′ is independently halo, C 1-4 alkyl which is optionally substituted with C 1-4 alkoxy, C 1-4 haloalkyl, or C 3-6 cycloalkyl.
• each R′ is independently fluoro, chloro, iodo, bromo, —CH 2 F, —CHF 2 , —CF 3 , fluoroethyl, difluoroethyl, trifluoroethyl, fluoropropyl, difluoropropyl, trifluoropropyl, methyl, ethyl, propyl, butyl, methoxymethyl, methoxyethyl, ethoxymethyl, methoxypropyl, ethoxyethyl, ethoxypropyl, cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl.
• each R′ is independently fluoro, chloro, methyl, —CH 2 F, —CHF 2 , —CF 3 , methoxyethyl, or cyclopropyl.
• each R′ is independently —NH 2 .
• each R′ is independently halo, —NH 2 , C 1-4 alkyl which is optionally substituted with C 1-4 alkoxy, C 1-4 haloalkyl, or C 3-6 cycloalkyl.
• each R′ is independently —NH 2 , fluoro, chloro, methyl, —CH 2 F, —CHF 2 , —CF 3 , methoxyethyl, or cyclopropyl.
• W is CH or N. In certain other embodiments, W is CH. In yet other embodiments, W is N.
• Each and every variation of W may be combined with each and every variation of n, m′, X, Y, Z, A′, R′, R 1 , R 2 , and R 3 as described above.
• n R 1 , R 2 , R 3 , and R 5 as described as formulae (I) and (J); m is 0, 1, or 2; p is 0, 1, 2, or 3; and R 4a is independently selected from halo, cyano, —NH 2 , and optionally substituted C 1-6 alkyl.
• p is 0. In certain embodiments, p is 1, 2, or 3. In some embodiments, p is 1 or 2. In some embodiments, p is 1 and R 4a moiety may be located on any position of the pyrimidinyl or pyrazinyl ring. In another embodiment, p is 2 and both R 4a substituents or moieties may be the same or different; each of the two R 4a moiety may be located on any position of the pyrimidinyl or pyrazinyl ring. In yet another embodiment, p is 3 and all R 4a substituents may be the same or different, or two R 4a may be the same and different from the third R 4a .
• each R 4a is independently selected from halo, —NH 2 , cyano, C 2-4 alkynyl, C 1-4 haloalkyl, and C 1-4 alkyl, wherein the C 2-4 alkynyl moiety is optionally substituted with C 6-10 aryl or C 4-8 heteroaryl, wherein each of the C 6-10 aryl or C 3-8 heteroaryl moieties is optionally substituted with one or two members independently selected from fluoro, chloro, bromo, iodo, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, difluoroethyl, and trifluoroethyl.
• each R 4a is independently selected from fluoro, chloro, bromo, iodo, cyano, —NH 2 , methyl, ethyl, propyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoroethyl, and difluoroethyl, wherein at least one R 4a is —NH 2 .
• p is 2 or 3, and at least one R 4a is —NH 2 .
• Each and every variation of p and R 4a may be combined with each and every variation of n, m, R 1 , R 2 , R 3 , and R 5 as described above.
• the compounds of the present application may bear one or more chiral centers.
• the compounds bearing the chiral center have the same molecular formula and the same chemical name with different stereoisomer designations.
• the below 2,4-diamino-6-((1-(5-chloro-4-oxo-3-(1H-pyrazol-3-yl)-3,4-dihydroquinazolin-2-yl)propyl)amino)pyrimidine-5-carbonitrile bearing one chiral center can be resolved into the (S) and (R) enantiomers, (S)-2,4-diamino-6-((1-(5-chloro-4-oxo-3-(1H-pyrazol-3-yl)-3,4-dihydroquinazolin-2-yl)propyl)amino)pyrimidine-5-carbonitrile and ((R)-2,4-diamino-6-((1-(5-chloro-4-o
• compound 1 in table 1 may be named as 2,4-diamino-6-[[(1S)-1-[5-chloro-4-oxo-3-(1H-pyrazol-3-yl)quinazolin-2-yl]propyl]amino]pyrimidine-5-carbonitrile or (S)-2,4-diamino-6-((1-(5-chloro-4-oxo-3-(1H-pyrazol-3-yl)-3,4-dihydroquinazolin-2-yl)propyl)amino)pyrimidine-5-carbonitrile using IUPAC or ChemBioDraw Ultra 12.0, respectively.
• the present application provides pharmaceutically acceptable salts, hydrates, solvates, isomers, tautomers, stereoisomers, enantiomers, racemates, atropisomers, polymorphs, prodrugs, or a mixture thereof, of the compounds described herein.
• the present application provides the compounds in which from 1 to n hydrogen atoms attached to a carbon atom may be replaced by a deuterium atom or D, in which n is the number of hydrogen atoms in the molecule. It is known that the deuterium atom is a non-radioactive isotope of the hydrogen atom.
• Such compounds may increase resistance to metabolism, and thus may be useful for increasing the half-life of the compounds of any of the formulae described herein or pharmaceutically acceptable salts, isomers, prodrugs, or solvates thereof, when administered to a mammal. See, e.g., Foster, “Deuterium Isotope Effects in Studies of Drug Metabolism”, Trends Pharmacol. Sci., 5(12):524-527 (1984).
• Such compounds are synthesized by means well known in the art, for example by employing starting materials in which one or more hydrogen atoms have been replaced by deuterium.
• a compound of the present application refers to a compound having the structure of any of the formulae (J), (I), (Ia), (Ib), (II), (IIa), (IIb), (III), (IIIa), (IIIb), (IV), (IVa), and (IVb).
• compounds of the present application are Compounds 1-291 as described herein.
• “Pharmaceutically acceptable” or “physiologically acceptable” refer to compounds, salts, compositions, dosage forms and other materials which are useful in preparing a pharmaceutical composition that is suitable for veterinary or human pharmaceutical use.
• “Pharmaceutically acceptable salts” or “physiologically acceptable salts” refer to salts of pharmaceutical compounds that retain the biological effectiveness and properties of the underlying compound, and which are not biologically or otherwise undesirable. There are acid addition salts and base addition salts. Pharmaceutically acceptable acid addition salts may be prepared from inorganic and organic acids. Acids and bases useful for reaction with an underlying compound to form pharmaceutically acceptable salts (acid addition or base addition salts respectively) are known to one of skill in the art.
• an addition salt particularly a pharmaceutically acceptable addition salt, may be produced by dissolving the free base in a suitable organic solvent and treating the solution with an acid, in accordance with conventional procedures for preparing acid addition salts from base compounds.
• “Isomers” refers to compounds that have the same molecular formula.
• the term isomers include double bond isomers, racemates, stereoisomers, enantiomers, diastereomers, and atropisomers.
• Single isomers, such as enantiomers or diastereomers, can be obtained by asymmetric synthesis or by resolution of a mixture of isomers. Resolution of a mixture of isomers (e.g. racemates) maybe accomplished, for example, by conventional methods such as crystallization in the presence of a resolving agent, or chromatography, using, for example a chiral high pressure liquid chromatography (HPLC) column.
• “Double bond isomers” refer to Z- and E-forms (or cis- and trans-forms) of the compounds with carbon-carbon double bonds.
• Atropisomers refers to conformational stereoisomers which occur when rotation about a single bond in the molecule is prevented, or greatly hindered, as a result of steric interactions with other parts of the molecule and the substituents at both ends of the single bond are asymmetrical, i.e., they do not require a stereocenter. Where the rotational barrier about the single bond is high enough, and interconversion between conformations is slow enough, separation and isolation of the isomeric species may be permitted. Atropisomers may be separated by the methods well known in the art. Unless otherwise indicated, the description is intended to include individual atropisomers as well as mixtures.
• the atropisomers may be represented by the same chemical name with different atropisomer designations.
• the below structures are atropisomers of compound 84, (S)-2,4-diamino-6-((1-(3-(4-bromo-1H-pyrazol-3-yl)-5-chloro-4-oxo-3,4-dihydroquinazolin-2-yl)ethyl)amino)pyrimidine-5-carbonitrile.
• Racemates refers to a mixture of enantiomers.
• Stereoisomers or “stereoisomeric forms” refer to compounds that differ in the chirality of one or more stereocenters. Stereoisomers include enantiomers and diastereomers. The compounds may exist in stereoisomeric form if they possess one or more asymmetric centers or a double bond with asymmetric substitution and, therefore, can be produced as individual stereoisomers or as mixtures. Unless otherwise indicated, the description is intended to include individual stereoisomers as well as mixtures. The methods for the determination of stereochemistry and the separation of stereoisomers are well-known in the art (see. e.g., Chapter 4 of Advanced Organic Chemistry, 4th ed., J. March, John Wiley and Sons, New York, 1992).
• Tautomers or “tautomeric formers” refer to alternate forms of a compound that differ in the position of a proton, such as enol-keto and imine-enamine tautomers, or heteroaryls such as pyrazoles, imidazoles, benzimidazoles, triazoles, and tetrazoles.
• a “solvate” is formed by the interaction of a solvent and a compound. Solvates of salts of the compounds of any of the formulae described herein are also provided. Hydrates of the compounds of any of the formulae are also provided.
• a “prodrug” is defined in the pharmaceutical field as a biologically inactive derivative of a drug that upon administration to the human body is converted to the biologically active parent drug according to some chemical or enzymatic pathway.
• the compound described herein or a pharmaceutically acceptable salt thereof is an (S)-enantiomer. In any one of the foregoing embodiments, the compound described herein or a pharmaceutically acceptable salt thereof is an (R)-enantiomer. In any one of the foregoing embodiments, the compound described herein or a pharmaceutically acceptable salt thereof is an atropisomer.
• the application also provides a composition containing a mixture of enantiomers of the compound or a pharmaceutically acceptable salt thereof.
• the mixture is a racemic mixture.
• the composition comprises the (S)-enantiomer of a compound in excess of over the corresponding the (R)-enantiomer of the compound.
• the composition contains the (S)-enantiomer of the compound and is substantially free of its corresponding (R)-enantiomer.
• a composition substantially free of the (R)-enantiomer has less than or about 40%, 35%, 30%, 25%, 20%, 15%, 10%, 5%, 1%, 0.05%, or 0.01% of the (R)-enantiomer.
• the composition containing the (S)-enantiomer of a compound or a pharmaceutically acceptable salt thereof predominates over its corresponding (R)-enantiomer by a molar ratio of at least or about 9:1, at least or about 19:1, at least or about 40:1, at least or about 80:1, at least or about 160:1, or at least or about 320:1.
• composition containing a compound according to any of the formulae described herein or a pharmaceutically acceptable salt thereof may also contain the compound in enantiomeric excess (e.e.).
• a compound with 95% (S)-isomer and 5% (R)-isomer will have an e.e. of 90%.
• the compound has an e.e. of at least or about 60%, 75%, 80%, 85%, 90%, 95%, 98% or 99%.
• the compound or a pharmaceutically acceptable salt thereof is an atropisomer.
• Another embodiment provides the composition containing a mixture of atropisomers of the compound or a pharmaceutically acceptable salt thereof.
• a compound with 95% of one atropisomer and 5% of the other atropisomers By way of example, a compound with 95% of one atropisomer and 5% of the other atropisomers.
• the application also provides the free base forms of the compounds described herein.
• provided herein are the enantiomers, (R) or (S), of the compounds of the formulae described herein.
• provided herein are the atropisomers of the compounds of the formulae described herein.
• compositions comprising the compounds described herein or a pharmaceutically acceptable salt, isomer, prodrug, or solvate thereof.
• the composition may include racemic mixtures, mixtures containing an enantiomeric excess of one enantiomer or single diastereomers or diastereomeric mixtures. All such isomeric forms of these compounds are expressly included herein, the same as if each and every isomeric form were specifically and individually listed.
• provided herein are also polymorphs, such as crystalline and amorphous forms, of the compounds described herein.
• provided are also chelates, non-covalent complexes, and mixtures thereof, of the compounds of the formula described herein or pharmaceutically acceptable salts, prodrugs, or solvates thereof.
• a “chelate” is formed by the coordination of a compound to a metal ion at two (or more) points.
• a “non-covalent complex” is formed by the interaction of a compound and another molecule wherein a covalent bond is not formed between the compound and the molecule. For example, complexation can occur through van der Waals interactions, hydrogen bonding, and electrostatic interactions (also called ionic bonding).
• the compounds of the formulae described herein or a pharmaceutically acceptable salt, isomer, prodrug, or solvate thereof may be used for the treatment of diseases and/or conditions mediated by PI3K isoforms.
• the application provides the compounds for use in therapy.
• methods for inhibiting one or more PI3K isoforms are provided.
• the application further provides methods for use in such methods.
• the PI3K isoforms may be selectively or specifically inhibited. Additionally, the compounds may be used to inhibit PI3K activity therapeutically or prophylactically, such as PI3K ⁇ and/or PI3K ⁇ .
• the compounds according to the present application may be used in combination with one or more additional therapeutic agents.
• the therapeutic agents may be in the forms of compounds, antibodies, polypeptides, or polynucleotides.
• the therapeutic agent includes, but is not limited to, a chemotherapeutic agent, an immunotherapeutic agent, a radiotherapeutic agent, an anti-neoplastic agent, an anti-cancer agent, an anti-proliferation agent, an anti-fibrotic agent, an anti-angiogenic agent, a therapeutic antibody, or any combination thereof.
• the application provides a product comprising a compound described herein and an additional therapeutic agent as a combined preparation for simultaneous, separate or sequential use in therapy, e.g. a method of treating a disease, disorder, or condition that is mediated by PI3K isoforms.
• the therapeutic agents may be those that inhibit or modulate the activities of Bruton's tyrosine kinase, spleen tyrosine kinase, apoptosis signal-regulating kinase, Janus kinase, lysyl oxidase, lysyl oxidase-like proteins, matrix metallopeptidase, bromodomain-containing protein, adenosine A2B receptor, isocitrate dehydrogenase, serine/threonine kinase TPL2, discoidin domain receptor, serine/threonine-protein kinases, IKK, MEK, EGFR, histone deacetylase, protein kinase C, or any combination thereof.
• the therapeutic agent may be selected from a PI3K (including PI3K ⁇ , PI3K ⁇ , PI3K ⁇ , PI3K ⁇ , and/or pan-PI3K) inhibitor, a JAK (Janus kinase, including JAK1, JAK2, and/or JAK3) inhibitor, a SYK (spleen tyrosine kinase) inhibitor, a BTK (Bruton's tyrosine kinase) inhibitor, an A2B (adenosine A2B receptor) inhibitor, an ACK (activated CDC kinase, including ACK1) inhibitor, an ASK (apoptosis signal-regulating kinase, including ASK1) inhibitor, Aurora kinase, a BRD (bromodomain-containing protein, including BRD4) inhibitor, a Bcl (B-cell CLL/lymphoma, including Bcl-1 and/or Bcl-2) inhibitor, a CAK (CDK), CDK
• the JAK inhibitor is N-(cyanomethyl)-4-[2-(4-morpholinoanilino)pyrimidin-4-yl]benzamide as named by ChemDraw (may also be referred to as CYT0387 or momelotinib) and may be synthesized by the methods described in U.S. Pat. No. 8,486,941.
• the SyK inhibitor is 6-(1H-indazol-6-yl)-N-(4-morpholinophenyl)imidazo[1,2-a]pyrazin-8-amine as named by ChemDraw (may also be referred to as 6-(1H-indazol-6-yl)-N-[4-(morpholin-4-yl)phenyl]imidazo[1,2-a]pyrazin-8-amine) and may be synthesized by the methods described in U.S. Pat. No. 8,450,321.
• the BTK inhibitor is (S)-6-amino-9-(1-(but-2-ynoyl)pyrrolidin-3-yl)-7-(4-phenoxyphenyl)-7H-purin-8(9H)-one as named by ChemDraw (may also be 6-amino-9-[(3R)-1-(2-butynoyl)-3-pyrrolidinyl]-7-(4-phenoxyphenyl)-7,9-dihydro-8H-purin-8-one) and may be synthesized by the methods in U.S. Pat. No. 8,557,803.
• Chemotherapeutic agents may be categorized by their mechanism of action into, for example, the following groups: anti-metabolites/anti-cancer agents, such as pyrimidine analogs (floxuridine, capecitabine, and cytarabine); purine analogs, folate antagonists and related inhibitors, antiproliferative/antimitotic agents including natural products such as vinca alkaloid (vinblastine, vincristine) and microtubule such as taxane (paclitaxel, docetaxel), vinblastin, nocodazole, epothilones and navelbine, epidipodophyllotoxins (etoposide, teniposide); DNA damaging agents (actinomycin, amsacrine, busulfan, carboplatin, chlorambucil, cisplatin, cyclophosphamide, Cytoxan, dactinomycin, daunorubicin, doxorubicin, epirubicin, iphosphamide,
• chemotherapeutic agent or “chemotherapeutic” (or “chemotherapy,” in the case of treatment with a chemotherapeutic agent) is meant to encompass any non-proteinaceous (i.e, non-peptidic) chemical compound useful in the treatment of cancer.
• chemotherapeutic agents include alkylating agents such as thiotepa and cyclophosphamide (CYTOXAN); alkyl sulfonates such as busulfan, improsulfan and piposulfan; aziridines such as benzodopa, carboquone, meturedopa, and uredopa; emylerumines and memylamelamines including alfretamine, triemylenemelamine, triethylenephosphoramide, triethylenethiophosphoramide and trimemylolomelamine; acetogenins (especially bullatacin and bullatacinone); a camptothecin (including synthetic analogue topotecan); bryostatin; callystatin; CC-1065 (including its adozelesin, carzelesin and bizclesin synthetic analogues); cryptophycins (particularly cryptophycin 1 and cryptophycin 8); dolastatin; duocarmycin (CY
• dynemicin including dynemicin A; bisphosphonates, such as clodronate; an esperamicin; as well as neocarzinostatin chromophore and related chromoprotein enediyne antibiotic chromomophores), aclacinomysins, actinomycin, authramycin, azaserine, bleomycins, cactinomycin, carabicin, carminomycin, carzinophilin, chromomycins, dactinomycin, daunorubicin, detorubicin, 6-diazo-5-oxo-L-norleucine, doxorubicin (including morpholino-doxorubicin, cyanomorpholino-doxorubicin, 2-pyrrolino-doxorubicin and deoxydoxorubicin), epirubicin, esorubicin
• chemotherapeutic agent include anti-hormonal agents that act to regulate or inhibit hormone action on tumors such as anti-estrogens and selective estrogen receptor modulators (SERMs), including, for example, tamoxifen (including NolvadexTM), raloxifene, droloxifene, 4-hydroxytamoxifen, trioxifene, keoxifene, LYI 17018, onapristone, and toremifene (Fareston®); inhibitors of the enzyme aromatase, which regulates estrogen production in the adrenal glands, such as, for example, 4(5)-imidazoles, aminoglutethimide, megestrol acetate (Megace®), exemestane, formestane, fadrozole, vorozole (Rivisor®), letrozole (Femara®), and anastrozole (Arimidex®); and anti-androgens such as flutamide, nilutamide,
• SERMs selective
• the anti-angiogenic agents include, but are not limited to, retinoid acid and derivatives thereof, 2-methoxyestradiol, ANGIOSTATIN®, ENDOSTATIN®, suramin, squalamine, tissue inhibitor of metalloproteinase-1, tissue inhibitor of metalloproternase-2, plasminogen activator inhibitor-1, plasminogen activator inhibitor-2, cartilage-derived inhibitor, paclitaxel (nab-paclitaxel), platelet factor 4, protamine sulphate (clupeine), sulphated chitin derivatives (prepared from queen crab shells), sulphated polysaccharide peptidoglycan complex (sp-pg), staurosporine, modulators of matrix metabolism, including for example, proline analogs ((1-azetidine-2-carboxylic acid (LACA), cishydroxyproline, d,l-3,4-dehydroproline, thiaproline, .alpha.-dipyrid
• anti-angiogenesis agents include antibodies, preferably monoclonal antibodies against these angiogenic growth factors: beta-FGF, alpha-FGF, FGF-5, VEGF isoforms, VEGF-C, HGF/SF and Ang-1/Ang-2. See Ferrara N. and Alitalo, K. “Clinical application of angiogenic growth factors and their inhibitors” (1999) Nature Medicine 5:1359-1364.
• the anti-fibrotic agents include, but are not limited to, the compounds such as beta-aminopropionitrile (BAPN), as well as the compounds disclosed in U.S. Pat. No. 4,965,288 to Palfreyman, et al., issued Oct. 23, 1990, entitled “Inhibitors of lysyl oxidase,” relating to inhibitors of lysyl oxidase and their use in the treatment of diseases and conditions associated with the abnormal deposition of collagen; U.S. Pat. No. 4,997,854 to Kagan, et al., issued Mar.
• BAPN beta-aminopropionitrile
• Exemplary anti-fibrotic agents also include the primary amines reacting with the carbonyl group of the active site of the lysyl oxidases, and more particularly those which produce, after binding with the carbonyl, a product stabilized by resonance, such as the following primary amines: emylenemamine, hydrazine, phenylhydrazine, and their derivatives, semicarbazide, and urea derivatives, aminonitriles, such as beta-aminopropionitrile (BAPN), or 2-nitroethylamine, unsaturated or saturated haloamines, such as 2-bromo-ethylamine, 2-chloroethylamine, 2-trifluoroethylamine, 3-bromopropylamine, p-halobenzylamines, selenohomocysteine lactone.
• primary amines reacting with the carbonyl group of the active site of the lysyl oxidases, and more particularly those which produce
• the anti-fibrotic agents are copper chelating agents, penetrating or not penetrating the cells.
• Exemplary compounds include indirect inhibitors such compounds blocking the aldehyde derivatives originating from the oxidative deamination of the lysyl and hydroxylysyl residues by the lysyl oxidases, such as the thiolamines, in particular D-penicillamine, or its analogues such as 2-amino-5-mercapto-5-methylhexanoic acid, D-2-amino-3-methyl-3-((2-acetamidoethyl)dithio)butanoic acid, p-2-amino-3-methyl-3-((2-aminoethyl)dithio)butanoic acid, sodium-4-((p-1-dimethyl-2-amino-2-carboxyethyl)dithio)butane sulphurate, 2-acetamidoethyl-2-acetamid
• the immunotherapeutic agents include and are not limited to therapeutic antibodies suitable for treating patients; such as abagovomab, adecatumumab, afutuzumab, alemtuzumab, altumomab, amatuximab, anatumomab, arcitumomab, bavituximab, bectumomab, bevacizumab, bivatuzumab, blinatumomab, brentuximab, cantuzumab, catumaxomab, cetuximab, citatuzumab, cixutumumab, clivatuzumab, conatumumab, daratumumab, drozitumab, duligotumab, dusigitumab, detumomab, dacetuzumab, dalotuzumab, ecromeximab, elotuzumab
• the application also provides method for treating a subject who is undergoing one or more standard therapies, such as chemotherapy, radiotherapy, immunotherapy, surgery, or combination thereof. Accordingly, one or more therapeutic agent or inhibitors may be administered before, during, or after administration of chemotherapy, radiotherapy, immunotherapy, surgery or combination thereof.
• lymphomas are reviewed in Cheson, B. D., Leonard, J. P., “Monoclonal Antibody Therapy for B-Cell Non-Hodgkin's Lymphoma” The New England Journal of Medicine 2008, 359(6), p. 613-626; and Wierda, W. G., “Current and Investigational Therapies for Patients with CLL” Hematology 2006, p. 285-294. Lymphoma incidence patterns in the United States is profiled in Morton, L. M., et al. “Lymphoma Incidence Patterns by WHO Subtype in the United States, 1992-2001 ” Blood 2006, 107(1), p. 265-276.
• immunotherapeutic agents include, but are not limited to, rituximab (such as Rituxan), alemtuzumab (such as Campath, MabCampath), anti-CD19 antibodies, anti-CD20 antibodies, anti-MN-14 antibodies, anti-TRAIL, Anti-TRAIL DR4 and DR5 antibodies, anti-CD74 antibodies, apolizumab, bevacizumab, CHIR-12.12, epratuzumab (hLL2-anti-CD22 humanized antibody), galiximab, ha20, ibritumomab tiuxetan, lumiliximab, milatuzumab, ofatumumab, PRO131921, SGN-40, WT-1 analog peptide vaccine, WT1 126-134 peptide vaccine, tositumomab, autologous human tumor-derived HSPPC-96, and veltuzumab.
• Additional immunotherapy agents includes using cancer vaccines based upon the genetic makeup of an individual
• chemotherapy agents include aldesleukin, alvocidib, antineoplaston AS2-1, antineoplaston A10, anti-thymocyte globulin, amifostine trihydrate, aminocamptothecin, arsenic trioxide, beta alethine, Bcl-2 family protein inhibitor ABT-263, ABT-199, BMS-345541, bortezomib (Velcade®), bryostatin 1, busulfan, carboplatin, campath-1H, CC-5103, carmustine, caspofungin acetate, clofarabine, cisplatin, Cladribine (Leustarin), Chlorambucil (Leukeran), Curcumin, cyclosporine, Cyclophosphamide (Cyloxan, Endoxan, Endoxana, Cyclostin), cytarabine, denileukin diftitox, dexamethasone, DT PACE, docetaxel
• the therapeutic treatments can be supplemented or combined with any of the abovementioned therapies with stem cell transplantation or treatment.
• One example of modified approach is radioimmunotherapy, wherein a monoclonal antibody is combined with a radioisotope particle, such as indium In 111, yttrium Y 90, iodine I-131.
• combination therapies include, but are not limited to, Iodine-131 tositumomab (Bexxar®), Yttrium-90 ibritumomab tiuxetan (Zevalin®), Bexxar® with CHOP.
• peripheral blood stem cell transplantation autologous hematopoietic stem cell transplantation, autologous bone marrow transplantation, antibody therapy, biological therapy, enzyme inhibitor therapy, total body irradiation, infusion of stem cells, bone marrow ablation with stem cell support, in vitro-treated peripheral blood stem cell transplantation, umbilical cord blood transplantation, immunoenzyme technique, pharmacological study, low-LET cobalt-60 gamma ray therapy, bleomycin, conventional surgery, radiation therapy, and nonmyeloablative allogeneic hematopoietic stem cell transplantation.
• the methods include administering a compound of the formula described herein or a pharmaceutically acceptable salt, isomer, prodrug, or solvate thereof, in a therapeutically effective amount to a human in need thereof.
• the method can be employed to treat a patient who has or is believed to have a disease or condition whose symptoms or pathology is mediated by expression or activity of PI3K ⁇ and/or PI3K ⁇ .
• the patient may be a mammal or a human. In certain embodiment, the patient may be a human.
• Treatment is an approach for obtaining beneficial or desired results including clinical results.
• beneficial or desired clinical results may include one or more of the following: a) inhibiting the disease or condition (e.g., decreasing one or more symptoms resulting from the disease or condition, and/or diminishing the extent of the disease or condition); b) slowing or arresting the development of one or more clinical symptoms associated with the disease or condition (e.g., stabilizing the disease or condition, preventing or delaying the worsening or progression of the disease or condition, and/or preventing or delaying the spread (e.g., metastasis) of the disease or condition); and/or c) relieving the disease, that is, causing the regression of clinical symptoms (e.g., ameliorating the disease state, providing partial or total remission of the disease or condition, enhancing the effect of another medication, delaying the progression of the disease, increasing the quality of life, and/or prolonging survival.
• a) inhibiting the disease or condition e.g., decreasing one or more symptoms resulting from the disease or
• Prevention or “preventing” mean any treatment of a disease or condition that causes the clinical symptoms of the disease or condition not to develop.
• Compounds may, in some embodiments, be administered to a subject (including a human) who is at risk or has a family history of the disease or condition.
• Subject or “patient” refer to an animal, such as a mammal (including a human), that has been or will be the object of treatment, observation or experiment. The methods described herein may be useful in human therapy and/or veterinary applications.
• the subject is a mammal.
• the subject is a human.
• “Human in need thereof” refers to a human who may have or is suspect to have diseases, or disorders, or conditions that would benefit from certain treatment; for example, being treated with the PI3K inhibitor of the compounds according to the present application.
• the subject may be a human who (i) has not received any treatment including chemotherapy treatment, (ii) is substantially refractory to at least one chemotherapy treatment, (iii) is in relapse after treatment with chemotherapy, or both (i) and (ii). In some of embodiments, the subject is refractory to at least one, at least two, at least three, or at least four chemotherapy treatments (including standard or experimental chemotherapies).
• a therapeutically effective amount or “effective amount” of a compound of the present application or a pharmaceutically acceptable salt, isomers, prodrug, or solvate thereof, mean an amount sufficient to effect treatment when administered to a subject, to provide a therapeutic benefit such as amelioration of symptoms or slowing of disease progression.
• a therapeutically effective amount may be an amount sufficient to decrease a symptom of a disease or condition responsive to inhibition of PI3K ⁇ and PI3K ⁇ activity.
• the therapeutically effective amount may vary depending on the subject, and disease or condition being treated, the weight and age of the subject, the severity of the disease or condition, and the manner of administering, which can readily be determined by one or ordinary skill in the art.
• the compounds described herein have the selectivity or selective inhibition to certain PI3K isoforms.
• the compounds have selectivity to PI3K ⁇ .
• the compounds have selectivity to PI3K ⁇ .
• the compounds have selectivity to PI3K ⁇ and PI3K ⁇ .
• the selectivity to PI3K isoforms may be determined by measuring the compound's activity in inhibiting certain PI3K isoforms using the assay described in the example below or the methods commonly used. It is understood that the conditions (e.g. the reagent concentration or the incubation temperature) may be varied and the results of the assay may vary. In some instances, the value may vary within a range of one to three-fold.
• inhibitors indicates a decrease in the baseline activity of a biological activity or process.
• inhibitor of activity of PI3K isoforms or variants thereof refer to a decrease in activity in any PI3K isoform (e.g., alpha, beta, gamma, or delta) as a direct or indirect response to the presence of a compound of any of the formula described herein relative to the activity of PI3K isoform in the absence of such compound.
• “Inhibition of PI3K ⁇ and/or PI3K ⁇ activities” or variants thereof refer to a decrease in PI3K ⁇ and/or PI3K ⁇ activities as a direct or indirect response to the presence of the compounds described herein, relative to the activities of PI3K ⁇ and/or PI3K ⁇ in the absence of such compound.
• the inhibition of PI3K isoform activities may be compared in the same subject prior to treatment, or other subjects not receiving the treatment.
• the decrease in the activity of PI3K may be due to the direct interaction of the compound with PI3K, or due to the interaction of the compounds described herein with one or more other factors that affect PI3K activity.
• the presence of the compounds may decrease the activities of PI3K ⁇ and/or PI3K ⁇ by directly binding to PI3K ⁇ and/or PI3K ⁇ , by causing (directly or indirectly) another factor to decrease PI3K ⁇ and/or PI3K ⁇ activities, or by (directly or indirectly) decreasing the amount of PI3K ⁇ and/or PI3K ⁇ present in the cell or organism.
• PI3K inhibitor or variant thereof refers to a compound that inhibits the activity of PI3K.
• PI3K isoform selective inhibitor or variant thereof refers to a compound that inhibits the activity of one or more PI3K isoforms more effectively than the other remaining PI3K isoforms.
• PI3K ⁇ selective inhibitor generally refers to a compound that inhibits the activity of the PI3K ⁇ isoform more effectively than other isoforms of the PI3K family
• PI3K ⁇ selective inhibitor generally refers to a compound that inhibits the activity of the PI3K ⁇ isoform more effectively than other isoforms of the PI3K family.
• PI3K ⁇ / ⁇ selective inhibitor generally refers to a compound that inhibits the activity of both PI3K ⁇ and PI3K ⁇ isoforms more effectively than other isoforms of the PI3K family (e.g., PI3K ⁇ or ⁇ ).
• the relative efficacies of compounds as inhibitors of an enzyme activity can be established by determining the concentrations at which each compound inhibits the activity to a predefined extent and then comparing the results.
• the efficacy of a compound as an inhibitor of one or more PI3K isoforms can be measured by the compound concentration that inhibits 50% of the activity in a biochemical assay, i.e., the 50% inhibitory concentration or “IC 50 ”.
• the determination of IC 50 values can be accomplished using conventional techniques known in the art, including the techniques described in the Examples below. In general, an IC 50 can be determined by measuring the activity of a given enzyme in the presence of a range of concentrations of the compound under the study.
• the experimentally obtained values of enzyme activity may then be plotted against the compound concentrations used.
• concentration of the inhibitor that shows 50% enzyme activity is taken as the IC 50 value.
• other inhibitory concentrations can be defined through appropriate determinations of activity. For example, in some settings it may be desirable to establish a 90% inhibitory concentration, i.e., IC 90 .
• a PI3K ⁇ selective inhibitor is a compound that exhibits a 50% inhibitory concentration (IC 50 ) with respect to PI3K ⁇ that is at least 10-fold, at least 20-fold, at least 30-fold, at least 50-fold, at least 100-fold, at least 200-fold, or at least 500-fold lower than the IC 50 with respect to either PI3K ⁇ or PI3K ⁇ or both PI3K ⁇ and PI3K ⁇ .
• IC 50 inhibitory concentration
• a PI3K ⁇ / ⁇ selective inhibitor is a compound that exhibits a 50% inhibitory concentration (IC 50 ) with respect to PI3K ⁇ and PI3K ⁇ that is at least 10-fold, at least 20-fold, at least 30-fold, at least 50-fold, at least 75-fold, at least 100-fold, at least 200-fold, and at least 500-fold lower than the IC 50 with respect to either PI3K ⁇ or PI3K ⁇ .
• the dual PI3K ⁇ / ⁇ selective inhibitor may have the same or similar IC 50 to both PI3K ⁇ and PI3K ⁇ or may have different IC 50 to either PI3K ⁇ or PI3K ⁇ .
• potency refers to the compound exhibiting an IC 50 value that is less than 100 nM. When comparing two compounds, the compound that exhibits a lower IC 50 value is referred to as a more potent inhibitor.
• the compounds of the present application exhibit unexpected selectivity to PI3K ⁇ .
• certain compounds in Table 1 exhibit low IC 50 values (e.g. 1 to 100 nM) to both PI3K ⁇ and PI3K ⁇ .
• Certain compounds in Table 1a also exhibited such selectivity to PI3K isoforms.
• certain compounds of formula (I) exhibited at least between 10-fold to 400-fold lower IC 50 values for PI3K ⁇ than PI3K ⁇ , suggesting the compounds exhibit more selectivity to PI3K ⁇ compared to PI3K ⁇ (i.e., inhibits the activity of the PI3K ⁇ isoform more effectively than the PI3K ⁇ isoform as shown by the PI3K ⁇ /PI3K ⁇ ratio).
• the compounds described herein exhibit selectivity to both PI3K ⁇ and PI3K ⁇ .
• ex vivo means within a living individual, as within an animal or human. In this context, the methods described herein may be used therapeutically in an individual.
• Ex vivo means outside of a living individual.
• ex vivo cell populations include in vitro cell cultures and biological samples including fluid or tissue samples obtained from individuals. Such samples may be obtained by methods well known in the art. Exemplary biological fluid samples include blood, cerebrospinal fluid, urine, and saliva. Exemplary tissue samples include tumors and biopsies thereof. In this context, the compounds may be used for a variety of purposes, including therapeutic and experimental purposes.
• PI3K selective inhibitor for example, it may be used ex vivo to determine the optimal schedule and/or dosing of administration of a PI3K selective inhibitor for a given indication, cell type, individual, and other parameters. Information gleaned from such use may be used for experimental purposes or in the clinic to set protocols for in vivo treatment. Other ex vivo uses for which the invention may be suited are described below or will become apparent to those skilled in the art.
• the compounds of the formula described herein or a pharmaceutically acceptable salt, prodrug, or solvate thereof may be further characterized to examine the safety or tolerance dosage in human or non-human subjects. Such properties may be examined using commonly known methods to those skilled in the art.
• PI3K ⁇ is generally expressed in hematopoietic cells. Also, PI3K ⁇ is generally mis-regulated in certain cancer cells. Aberrant proliferation of cells often interferes with normal tissue function, which may result in abnormal cellular response such as immunity, inflammation, and/or apoptosis.
• the selective inhibitors to PI3K ⁇ and/or PI3K ⁇ are useful in treating, inhibiting, or preventing aberrant proliferation of cancerous and/or hematopoietic cells and ameliorating the symptoms and secondary conditions.
• the compounds described herein may be used to treat subjects having various disease states, disorders, and conditions (also collectively referred to as “indications”) associated with PI3K isoforms or their activities.
• indications may include, for example, cancer, including hematologic malignancies (e.g. leukemias and lymphomas, myeloproliferative disorders, myelodysplastic syndromes, plasma cell neoplasms) and solid tumors, inflammation, fibrosis, allergic conditions (including hypersensitivity), cardiovascular diseases, neurodegenerative diseases, renal disorders, viral infections, obesity, and autoimmune diseases.
• the compounds described herein may be used to treat cancers that are mediated by, dependent on, or associated with PI3K activity.
• the disease or condition is an autoimmune disease, an inflammatory disease, or a cancer.
• the disease or condition is chosen from rheumatoid arthritis, osteoarthritis, atherosclerosis, psoriasis, systemic lupus erythematosus, multiple sclerosis, inflammatory bowel disease, asthma, chronic obstructive airways disease, pneumonitis, dermatitis, alopecia, nephritis, vasculitis, atherosclerosis, Alzheimer's disease, hepatitis, primary biliary cirrhosis, sclerosing cholangitis, diabetes (including type I diabetes), acute rejection of transplanted organs, lymphomas, multiple myelomas, leukemias, neoplasms and solid tumors.
• the disease is a solid tumor.
• the solid tumor includes but is not limited to pancreatic cancer, bladder cancer, colorectal cancer, breast cancer, prostate cancer, renal cancer, hepatocellular cancer, lung cancer, ovarian cancer, cervical cancer, rectum cancer, liver cancer, kidney cancer, stomach cancer, skin cancer, gastric cancer, esophageal cancer, head and neck cancer, melanoma, neuroendocrine cancers, CNS cancers (e.g., neuroblastoma), brain tumors (e.g., glioma, anaplastic oligodendroglioma, adult glioblastoma multiforme, and adult anaplastic astrocytoma), bone cancer, or soft tissue sarcoma.
• the solid tumor is non-small cell lung cancer, small-cell lung cancer, colon cancer, CNS cancer, melanoma, ovarian cancer, renal cancer, pancreatic cancer, prostate cancer, or breast cancer.
• the present application also provides a method for treating a human in need thereof, who has or is suspected of having a disease or condition responsive or believed to be responsive to the inhibition of PI3K ⁇ and/or PI3K ⁇ activity by administering to the subject a compound of the formulae described herein or a pharmaceutically acceptable salt, enantiomer, atropisomer, tautomer, prodrug, or solvate thereof.
• the application provides a method of inhibiting kinase activity of a PI3K ⁇ and/or PI3K ⁇ polypeptides by contacting the polypeptides with a compound of the formulae described herein or a pharmaceutically acceptable salt, isomer, prodrug, solvate, or a mixture thereof.
• the application provides a method of decreasing cell viability, increasing cell death or apoptosis, increasing interference with PI3K signaling pathways (including AKT, S6RP, ERK phosphorylation), and/or reduction in chemokine production with an effective amount of a compound of any of the formulae described herein or a pharmaceutically acceptable salt, isomer, prodrug, solvate, or a mixture thereof.
• the application further provides a method of disrupting leukocyte function comprising contacting the leukocytes with an effective amount of a compound of any of the formulae described herein or a pharmaceutically acceptable salt, isomer, prodrug, solvate, or a mixture thereof, in a human in need thereof.
• a method of inhibiting growth or proliferation of cancer cells comprising contacting the cancer cells with an effective amount of a compound of the formulae described herein or a pharmaceutically acceptable salt, isomer, prodrug, solvate, or a mixture thereof.
• kits that include a compound of the formulae of the present application or a pharmaceutically acceptable salt, isomer, prodrug, or solvate thereof, and suitable packaging.
• a kit further includes instructions for use.
• a kit includes a compound of the formulae described herein or a pharmaceutically acceptable salt, isomer, prodrug, or solvate thereof, and a label and/or instructions for use of the compounds in the treatment of the indications, including the diseases or conditions, described herein.
• articles of manufacture that include a compound of any of the formulae described herein or a pharmaceutically acceptable salt, isomer, prodrug, or solvate thereof, in a suitable container.
• the container may be a vial, jar, ampoule, preloaded syringe, and intravenous bag.
• compositions that contain one or more of the compounds of any of the formulae disclosed herein or a pharmaceutically acceptable salt, isomers, prodrug, or solvate thereof, and one or more pharmaceutically acceptable vehicles selected from carriers, adjuvants and excipients.
• suitable pharmaceutically acceptable vehicles may include, for example, inert solid diluents and fillers, diluents, including sterile aqueous solution and various organic solvents, permeation enhancers, solubilizers and adjuvants.
• Such compositions are prepared in a manner well known in the pharmaceutical art.
• the pharmaceutical compositions may be administered in either single or multiple doses.
• the pharmaceutical composition may be administered by various methods including, for example, rectal, buccal, intranasal and transdermal routes.
• the pharmaceutical composition may be administered by intra-arterial injection, intravenously, intraperitoneally, parenterally, intramuscularly, subcutaneously, orally, topically, or as an inhalant.
• the pharmaceutical composition is administered orally.
• Oral administration may be another route for administration of the compounds described herein. Administration may be via, for example, capsule or enteric coated tablets.
• the active ingredient is usually diluted by an excipient and/or enclosed within such a carrier that can be in the form of a capsule, sachet, paper or other container.
• the excipient serves as a diluent, it can be in the form of a solid, semi-solid, or liquid material, which acts as a vehicle, carrier or medium for the active ingredient.
• compositions can be in the form of tablets, pills, powders, lozenges, sachets, cachets, elixirs, suspensions, emulsions, solutions, syrups, aerosols (as a solid or in a liquid medium), ointments containing, for example, up to 10% by weight of the active compound, soft and hard gelatin capsules, sterile injectable solutions, and sterile packaged powders.
• the pharmaceutical composition is in the form of tablets.
• excipients include lactose, dextrose, sucrose, sorbitol, mannitol, starches, gum acacia, calcium phosphate, alginates, tragacanth, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, sterile water, syrup, and methyl cellulose.
• the formulations can additionally include lubricating agents such as talc, magnesium stearate, and mineral oil; wetting agents; emulsifying and suspending agents; preserving agents such as methyl and propylhydroxy-benzoates; sweetening agents; and flavoring agents.
• compositions that include at least one compound of any of the formulae described herein or a pharmaceutically acceptable salt, isomer, prodrug, or solvate thereof, can be formulated so as to provide quick, sustained or delayed release of the active ingredient after administration to the subject by employing procedures known in the art.
• Controlled release drug delivery systems for oral administration include osmotic pump systems and dissolutional systems containing polymer-coated reservoirs or drug-polymer matrix formulations. Examples of controlled release systems are given in U.S. Pat. Nos. 3,845,770; 4,326,525; 4,902,514; and 5,616,345.
• Another formulation for use in the methods of the present invention employs transdermal delivery devices (“patches”).
• transdermal patches may be used to provide continuous or discontinuous infusion of the compounds described herein in controlled amounts.
• the construction and use of transdermal patches for the delivery of pharmaceutical agents is well known in the art. See, e.g., U.S. Pat. Nos. 5,023,252, 4,992,445 and 5,001,139.
• Such patches may be constructed for continuous, pulsatile, or on demand delivery of pharmaceutical agents.
• the principal active ingredient may be mixed with a pharmaceutical excipient to form a solid preformulation composition containing a homogeneous mixture of a compound of any of the above formulae or a pharmaceutically acceptable salt, prodrug, or solvate thereof.
• a pharmaceutical excipient for preparing solid compositions such as tablets, the principal active ingredient may be mixed with a pharmaceutical excipient to form a solid preformulation composition containing a homogeneous mixture of a compound of any of the above formulae or a pharmaceutically acceptable salt, prodrug, or solvate thereof.
• the active ingredient may be dispersed evenly throughout the composition so that the composition may be readily subdivided into equally effective unit dosage forms such as tablets, pills and capsules.
• the tablets or pills of the compounds described herein may be coated or otherwise compounded to provide a dosage form affording the advantage of prolonged action, or to protect from the acid conditions of the stomach.
• the tablet or pill can include an inner dosage and an outer dosage component, the latter being in the form of an envelope over the former.
• the two components can be separated by an enteric layer that serves to resist disintegration in the stomach and permit the inner component to pass intact into the duodenum or to be delayed in release.
• enteric layers or coatings such materials including a number of polymeric acids and mixtures of polymeric acids with such materials as shellac, cetyl alcohol, and cellulose acetate.
• compositions for inhalation or insufflation may include solutions and suspensions in pharmaceutically acceptable, aqueous or organic solvents, or mixtures thereof, and powders.
• the liquid or solid compositions may contain suitable pharmaceutically acceptable excipients as described supra.
• the compositions are administered by the oral or nasal respiratory route for local or systemic effect.
• compositions in pharmaceutically acceptable solvents may be nebulized by use of inert gases. Nebulized solutions may be inhaled directly from the nebulizing device or the nebulizing device may be attached to a facemask tent, or intermittent positive pressure breathing machine. Solution, suspension, or powder compositions may be administered, preferably orally or nasally, from devices that deliver the formulation in an appropriate manner.
• a dosage may be expressed as a number of milligrams of a compound of the formula per kilogram of the subject's body weight (mg/kg). Dosages of between about 0.01 and 200 mg/kg may be appropriate. In some embodiments, about 0.01 and 150 mg/kg may be appropriate. In other embodiments a dosage of between 0.05 and 100 mg/kg may be appropriate.
• Normalizing according to the subject's body weight is particularly useful when adjusting dosages between subjects of widely disparate size, such as occurs when using the drug in both children and adult humans or when converting an effective dosage in a non-human subject such as dog to a dosage suitable for a human subject.
• the daily dosage may also be described as a total amount of a compound of the formulae administered per dose or per day.
• Daily dosage of a compound may be between about 1 mg and 2,000 mg, between about 1,000 to 2,000 mg/day, between about 1 to 1,000 mg/day, between about 1 to 500 mg/day, between about 100 to 150 mg/day, between about 1 to 100 mg/day, between about between about 1 to 50 mg/day, between about 50 to 100 mg/day, between about 100 to 125 mg/day, between about 100 to 150 mg/day, between about 100 to 175 mg/day, between about 100 to 200 mg/day, between about 100 to 225 mg/day, between about 100 to 250 mg/day, between about 100 to 350 mg/day, between about 100 to 400 mg/day, between about 100 to 450 mg/day, or between about 100 to 500 mg/day.
• the total daily dosage for a human subject may be between 1 mg and 1,000 mg/day, between about 1 to 100 mg/day, between about 1 to 50 mg/day, between about 50 to 100 mg/day, between 100 to 200 mg/day, between about 200 to 300 mg/day, between about 300 to 400 mg/day, between about 400 to 500 mg/day, between about 100 to 150 mg/day, between about 150 to 200 mg/day, between about 200 to 250 mg/day, between about 75 to 150 mg/day, or between about 150 to 300 mg/day.
• the compounds of the present application or the compositions thereof may be administered once, twice, three, or four times daily, using any suitable mode described above. Also, administration or treatment with the compounds according to any of the formulae described herein may be continued for a number of days; for example, commonly treatment would continue for at least 7 days, 14 days, or 28 days, for one cycle of treatment. In some treatment, the compound or the composition thereof is administered continuously, i.e. every day. Treatment cycles are well known in cancer chemotherapy, and are frequently alternated with resting periods of about 1 to 28 days, commonly about 7 days or about 14 days, between cycles. The treatment cycles, in other embodiments, may also be continuous.
• the method comprises administering to the subject an initial daily dose of about 1 to 500 mg of a compound of the above formula and increasing the dose by increments until clinical efficacy is achieved. Increments of about 1, 5, 10, 25, 50, 75, or 100 mg can be used to increase the dose. The dosage can be increased daily, every other day, twice per week, or once per week.
• the compounds of the present application may be prepared using the methods disclosed herein and routine modifications thereof, which will be apparent given the disclosure herein and methods well known in the art. Conventional and well-known synthetic methods may be used in addition to the teachings herein.
• the synthesis of typical compounds described herein may be accomplished as described in the following examples. If available, reagents may be purchased commercially, e.g., from Sigma Aldrich or other chemical suppliers. In general, compounds described herein are typically stable and isolatable at room temperature and pressure.
• Typical embodiments of compounds described herein may be synthesized using the general reaction schemes described below. It will be apparent given the description herein that the general schemes may be altered by substitution of the starting materials with other materials having similar structures to result in products that are correspondingly different. Descriptions of syntheses follow to provide numerous examples of how the starting materials may vary to provide corresponding products. Given a desired product for which the substituent groups are defined, the necessary starting materials generally may be determined by inspection. Starting materials are typically obtained from commercial sources or synthesized using published methods. For synthesizing compounds which are embodiments described in the present disclosure, inspection of the structure of the compound to be synthesized will provide the identity of each substituent group. The identity of the final product will generally render apparent the identity of the necessary starting materials by a simple process of inspection, given the examples herein.
• solvent refers to a solvent inert under the conditions of the reaction being described in conjunction therewith (including, for example, benzene, toluene, acetonitrile, tetrahydrofuran (“THF”), dimethylformamide (“DMF”), chloroform, methylene chloride (or dichloromethane), diethyl ether, methanol, and the like).
• solvents used in the reactions of the present invention are inert organic solvents, and the reactions are carried out under an inert gas, preferably nitrogen.
• the compounds of formula (J) may be prepared using the method shown in Reaction Scheme I. Also, the compounds of formula (I) may be prepared using the method shown below.
• the compound of formula (1) can be made by treating 5-substituted-2,4,6-trihalopyrimidine (A) with ammonium hydroxide in a suitable solvent such as dioxane, where G is halo (e.g. iodo, bromo, chloro or fluoro).
• A 5-substituted-2,4,6-trihalopyrimidine
• G is halo (e.g. iodo, bromo, chloro or fluoro).
• the reaction is carried out between 30° C. and 80° C. for between 2 and 8 hours or until the reaction is complete.
• water is added to the cooled solution, and the precipitate is collected by filtration.
• the nitrile may be converted to the carboxamide using commonly known methods.
• the compound of formula (2) can be made by combining compounds (B), (C) and (D) in the presence of a dehydrating agent.
• Compounds (B), (C) and (D) may be obtained commercially or made by the methods known in the art.
• X, Y, Z, n, m′, R 1 , R 2 , R 3 , and R 5 are defined as above.
• Compound (B) is mixed with Compound (D) in the presence of a coupling agent such as diphenyl phosphite in a solvent such as pyridine. After stirring at a temperature between ambient (i.e. room temperature) and 100° C. for between 1 and 5 hours, compound (C) is added. After further stirring at a temperature between ambient and 100° C.
• the reaction mixture is cooled to room temperature.
• an organic solvent such as ethyl acetate (EtOAc) may be added, followed by washing with mild base, water, and brine.
• the organic phase may be concentrated to obtain the compound of formula (2).
• the compound of formula (2) may be purified by any suitable method known in the art, such as chromatography on silica gel. Alternatively, the compound of formula (2) is purified directly without an aqueous work-up. Alternatively, the compound of formula (2) may be used in the next step without purification. Alkylsulfonyl and cyano compounds may be prepared using commonly known methods by displacing a halogen from the corresponding halogen containing compounds. In some cases, compounds (C) may be protected with groups such as triphenylmethyl, Boc, or trimethylsilyloxymethyl and removed in a subsequent step by commonly known methods.
• the compound of formula (3) can be made by removing the protecting group(s) from the compound of formula (2).
• the compound of formula (2) is dissolved in a suitable solvent and treated (i.e. mixed) with a suitable acid.
• suitable solvents may include, for example, dichloromethane, dioxane, or other suitable solvents.
• Suitable acids may include, for example, trifluoroacetic acid or hydrochloric acid.
• the reaction may be carried out at temperatures between ⁇ 78° C. to ambient temperature. On reaction completion, solvent is removed to obtain the compound of formula (3).
• the compound of formula (I-1) may generally be prepared by coupling compound of formula (3) and compound of formula (1) in the presence of a suitable base in a suitable solvent.
• the compound of formula (J), wherein A is a single bond may generally be prepared by coupling compound of formula (3) and compound of formula (1) in the presence of a suitable base in a suitable solvent.
• a suitable base may be by example, diisopropylethylamine.
• a suitable solvent may by example be isopropanol (IPA), DMSO, DMF, ethylene glycol, or ethanol.
• the reaction is typically performed at a temperature between 50° C. to 150° C. for about 30 minutes to 24 hours. Alternatively, the reaction may be conducted by microwave at a temperature between 100° C. to 150° C.
• the compound of formula (I-2) may generally be prepared by coupling a compound of formula (3) with a suitable acid in the presence of a coupling agent, such as HATU, DCC, or carbonyl diimidazole in the presence of a base such as triethylamine or diisopropylethylamine in a suitable solvent such as dichloromethane or THF.
• a coupling agent such as HATU, DCC, or carbonyl diimidazole
• a base such as triethylamine or diisopropylethylamine in a suitable solvent such as dichloromethane or THF.
• the compound of formula (I-2), wherein A is C(O) may generally be prepared by coupling a compound of formula (3) with a suitable acid in the presence of a coupling agent, such as HATU, DCC, or carbonyl diimidazole in the presence of a base such as triethylamine or diisopropylethylamine in a suitable solvent such as dichloromethane or THF.
• a coupling agent such as HATU, DCC, or carbonyl diimidazole
• a base such as triethylamine or diisopropylethylamine in a suitable solvent such as dichloromethane or THF.
• the resulting compound may be isolated by methods known in the art; for example, by removal of solvent under reduced pressure or aqueous work-up.
• the product may be purified using any suitable methods known in the art; for example, chromatography of the residue on a silica column, chromatography on an HPLC, or crystallization.
• the compounds may be isolated in the form of a free base or a salt (which includes and is not limited to a hydrochloric acid salt form or a trifluoroacetic acid salt form) and characterized by NMR.
• a salt which includes and is not limited to a hydrochloric acid salt form or a trifluoroacetic acid salt form
• the resulting compounds and their NMR characterizations may be either the free base or salt. The ratio of parent and corresponding salt is not determined.
• Trifluoroacetic acid (0.5 mL) was added to a suspension of(S)-tert-butyl (1-(5-chloro-4-oxo-3-(1H-pyrazol-3-yl)-3,4-dihydroquinazolin-2-yl)ethyl)carbamate (120 mg, 0.31 mmol) in dichloromethane (2.0 mL). The solution was stirred at room temperature for 3 hours and concentrated in vacuo. Dichloromethane (3.5 mL) was then added and the resulting solution was transferred to a flask containing 2-aminopyrazolo[1,5-a]pyrimidine-3-carboxylic acid (60 mg, 0.34 mmol).
• TR-FRET time-resolved fluorescence resonance energy transfer
• Class I PI3K isoforms were expressed and purified as heterodimeric recombinant proteins. All assay reagents and buffers for the TR-FRET assay were purchased from Millipore. PI3K isoforms were assayed under initial rate conditions in the presence of 25 mM Hepes (pH 7.4), and 2 ⁇ Km ATP (75-500 ⁇ M), 2 ⁇ M PIP2, 5% glycerol, 5 mM MgCl 2 , 50 mM NaCl, 0.05% (v/v) Chaps, 1 mM dithiothreitol, and 1% (v/v) DMSO at the following concentrations for each isoform: PI3K ⁇ , PI3K ⁇ , and PI3K ⁇ between 25 and 50 pM, and PI3K ⁇ at 2 nM.
• results were normalized based on positive (1 ⁇ M wortmanin) and negative (DMSO) controls, and the IC 50 values for PI3K ⁇ , ⁇ , ⁇ , and ⁇ were calculated from the fit of the dose-response curves to a four-parameter equation. These assays generally produced results within 3-fold of the reported mean.
• Table 2 summarizes the IC 50 (nM) values for PI3K isoforms ⁇ , ⁇ , and ⁇ . The results indicate that certain compounds of formula (I) inhibit both PI3K ⁇ and PI3K ⁇ . Also, Compound X exhibited PI3K ⁇ IC 50 of 0.2 nM, PI3K ⁇ IC 50 of 11 nM, PI3K ⁇ IC 50 of 7 nM. The PI3K ⁇ /PI3K ⁇ ratio for Compound X is 0.6. The results indicate that certain compounds have greater selectivity for PI3K ⁇ over PI3K ⁇ compared to compound X. Compounds of Table 1a were analyzed using the same assay, and the results are summarized in Table 2a.

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